Canonical Allele Identifier: CA1873825296

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402711_114402712delinsAC , CM000671.2:g.114402711_114402712delinsAC	GRCh38
NC_000009.11:g.117164991_117164992delinsAC , CM000671.1:g.117164991_117164992delinsAC	GRCh37
NC_000009.10:g.116204812_116204813delinsAC	NCBI36
NG_016700.1:g.107745_107746delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.1110_1111delinsGT	ENSP00000514396.1:n.1110_1111delinsGT
ENST00000362057.4:c.*42_*43delinsGT MANE Select	ENSP00000354623.3:n.*42_*43delinsGT
ENST00000674036.8:c.1739_1740delinsGT
ENST00000674048.1:n.2647_2648delinsGT
ENST00000265134.10:c.*42_*43delinsGT	ENSP00000265134.6:n.*42_*43delinsGT
ENST00000362057.3:c.*42_*43delinsGT	ENSP00000354623.3:n.*42_*43delinsGT
ENST00000374059.7:c.*42_*43delinsGT	ENSP00000363172.3:n.*42_*43delinsGT
NM_001083885.2:c.*42_*43delinsGT	NP_001077354.2:n.*42_*43delinsGT
NM_001173425.1:c.*42_*43delinsGT	NP_001166896.1:n.*42_*43delinsGT
NM_015404.3:c.*42_*43delinsGT	NP_056219.3:n.*42_*43delinsGT
XM_005251897.3:c.*42_*43delinsGT	XP_005251954.2:n.*42_*43delinsGT
XM_011518484.1:c.*42_*43delinsGT	XP_011516786.1:n.*42_*43delinsGT
XM_011518485.1:c.*42_*43delinsGT	XP_011516787.1:n.*42_*43delinsGT
XM_011518486.1:c.*42_*43delinsGT	XP_011516788.1:n.*42_*43delinsGT
XM_011518487.1:c.*42_*43delinsGT	XP_011516789.1:n.*42_*43delinsGT
XM_011518488.1:c.*42_*43delinsGT	XP_011516790.1:n.*42_*43delinsGT
XM_011518495.1:c.*42_*43delinsGT	XP_011516797.1:n.*42_*43delinsGT
NM_001346890.1:c.*42_*43delinsGT	NP_001333819.1:n.*42_*43delinsGT
XM_011518486.2:c.*42_*43delinsGT	XP_011516788.1:n.*42_*43delinsGT
XM_011518487.2:c.*42_*43delinsGT	XP_011516789.1:n.*42_*43delinsGT
XM_011518488.2:c.*42_*43delinsGT	XP_011516790.1:n.*42_*43delinsGT
NM_015404.4:c.*42_*43delinsGT MANE Select	NP_056219.3:n.*42_*43delinsGT
NM_001173425.2:c.*42_*43delinsGT	NP_001166896.1:n.*42_*43delinsGT
NM_001083885.3:c.*42_*43delinsGT	NP_001077354.2:n.*42_*43delinsGT