Canonical Allele Identifier: CA1873835876

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114425882_114425886delinsCTCTT , CM000671.2:g.114425882_114425886delinsCTCTT	GRCh38
NC_000009.11:g.117188162_117188166delinsCTCTT , CM000671.1:g.117188162_117188166delinsCTCTT	GRCh37
NC_000009.10:g.116227983_116227987delinsCTCTT	NCBI36
NG_016700.1:g.84571_84575delinsAAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699486.1:c.890+325_890+329delinsAAGAG	ENSP00000514397.1:n.890+325_890+329delinsAAGAG
ENST00000362057.4:c.1166+325_1166+329delinsAAGAG MANE Select	ENSP00000354623.3:n.1166+325_1166+329delinsAAGAG
ENST00000673811.1:n.1239_1243delinsAAGAG
ENST00000674036.8:c.349+325_349+329delinsAAGAG
ENST00000674048.1:n.186_190delinsAAGAG
ENST00000265134.10:c.17+325_17+329delinsAAGAG	ENSP00000265134.6:n.17+325_17+329delinsAAGAG
ENST00000362057.3:c.1166+325_1166+329delinsAAGAG	ENSP00000354623.3:n.1166+325_1166+329delinsAAGAG
ENST00000374059.7:c.-749_-745delinsAAGAG	ENSP00000363172.3:n.-749_-745delinsAAGAG
NM_001083885.2:c.17+325_17+329delinsAAGAG	NP_001077354.2:n.17+325_17+329delinsAAGAG
NM_001173425.1:c.1166+325_1166+329delinsAAGAG	NP_001166896.1:n.1166+325_1166+329delinsAAGAG
NM_015404.3:c.1166+325_1166+329delinsAAGAG	NP_056219.3:n.1166+325_1166+329delinsAAGAG
XM_005251897.3:c.964-17868_964-17864delinsAAGAG	XP_005251954.2:n.964-17868_964-17864delinsAAGAG
XM_011518484.1:c.1166+325_1166+329delinsAAGAG	XP_011516786.1:n.1166+325_1166+329delinsAAGAG
XM_011518485.1:c.1166+325_1166+329delinsAAGAG	XP_011516787.1:n.1166+325_1166+329delinsAAGAG
XM_011518486.1:c.1166+325_1166+329delinsAAGAG	XP_011516788.1:n.1166+325_1166+329delinsAAGAG
XM_011518487.1:c.1040+325_1040+329delinsAAGAG	XP_011516789.1:n.1040+325_1040+329delinsAAGAG
XM_011518488.1:c.1166+325_1166+329delinsAAGAG	XP_011516790.1:n.1166+325_1166+329delinsAAGAG
XM_011518489.1:c.1166+325_1166+329delinsAAGAG	XP_011516791.1:n.1166+325_1166+329delinsAAGAG
XM_011518490.1:c.1166+325_1166+329delinsAAGAG	XP_011516792.1:n.1166+325_1166+329delinsAAGAG
XM_011518491.1:c.1166+325_1166+329delinsAAGAG	XP_011516793.1:n.1166+325_1166+329delinsAAGAG
XM_011518492.1:c.1166+325_1166+329delinsAAGAG	XP_011516794.1:n.1166+325_1166+329delinsAAGAG
XM_011518493.1:c.1166+325_1166+329delinsAAGAG	XP_011516795.1:n.1166+325_1166+329delinsAAGAG
XM_011518494.1:c.1166+325_1166+329delinsAAGAG	XP_011516796.1:n.1166+325_1166+329delinsAAGAG
XM_011518495.1:c.-157-862_-157-858delinsAAGAG	XP_011516797.1:n.-157-862_-157-858delinsAAGAG
XR_929747.1:n.1874+325_1874+329delinsAAGAG
XR_929748.1:n.1874+325_1874+329delinsAAGAG
XR_929749.1:n.1874+325_1874+329delinsAAGAG
XR_929750.1:n.1874+325_1874+329delinsAAGAG
XR_929751.1:n.1874+325_1874+329delinsAAGAG
XR_929752.1:n.1874+325_1874+329delinsAAGAG
XR_929753.1:n.1874+325_1874+329delinsAAGAG
XR_929754.1:n.1874+325_1874+329delinsAAGAG
XR_929755.1:n.1874+325_1874+329delinsAAGAG
XR_929756.1:n.1874+325_1874+329delinsAAGAG
XR_929757.1:n.1874+325_1874+329delinsAAGAG
NM_001346890.1:c.-749_-745delinsAAGAG	NP_001333819.1:n.-749_-745delinsAAGAG
XM_011518486.2:c.1166+325_1166+329delinsAAGAG	XP_011516788.1:n.1166+325_1166+329delinsAAGAG
XM_011518487.2:c.1040+325_1040+329delinsAAGAG	XP_011516789.1:n.1040+325_1040+329delinsAAGAG
XM_011518488.2:c.1166+325_1166+329delinsAAGAG	XP_011516790.1:n.1166+325_1166+329delinsAAGAG
XM_011518489.3:c.1166+325_1166+329delinsAAGAG	XP_011516791.1:n.1166+325_1166+329delinsAAGAG
XM_011518491.3:c.1166+325_1166+329delinsAAGAG	XP_011516793.1:n.1166+325_1166+329delinsAAGAG
XM_011518492.2:c.1166+325_1166+329delinsAAGAG	XP_011516794.1:n.1166+325_1166+329delinsAAGAG
XM_011518494.3:c.1166+325_1166+329delinsAAGAG	XP_011516796.1:n.1166+325_1166+329delinsAAGAG
XR_929747.2:n.1185+325_1185+329delinsAAGAG
XR_929748.2:n.1185+325_1185+329delinsAAGAG
XR_929749.2:n.1185+325_1185+329delinsAAGAG
XR_929750.3:n.1185+325_1185+329delinsAAGAG
XR_929752.2:n.1185+325_1185+329delinsAAGAG
XR_929753.3:n.1185+325_1185+329delinsAAGAG
XR_929754.2:n.1185+325_1185+329delinsAAGAG
XR_929755.3:n.1185+325_1185+329delinsAAGAG
XR_929756.2:n.1185+325_1185+329delinsAAGAG
XR_929757.2:n.1185+325_1185+329delinsAAGAG
NM_015404.4:c.1166+325_1166+329delinsAAGAG MANE Select	NP_056219.3:n.1166+325_1166+329delinsAAGAG
NM_001173425.2:c.1166+325_1166+329delinsAAGAG	NP_001166896.1:n.1166+325_1166+329delinsAAGAG
NM_001083885.3:c.17+325_17+329delinsAAGAG	NP_001077354.2:n.17+325_17+329delinsAAGAG