Canonical Allele Identifier: CA1873827896

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114408063A= , CM000671.2:g.114408063A=	GRCh38
NC_000009.11:g.117170343A= , CM000671.1:g.117170343A=	GRCh37
NC_000009.10:g.116210164A=	NCBI36
NG_016700.1:g.102394T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362057.4:c.1627-45T= MANE Select	ENSP00000354623.3:n.1627-45T=
ENST00000673811.1:n.2351-45T=
ENST00000674036.8:c.600-45T=
ENST00000674048.1:n.1508-45T=
ENST00000265134.10:c.478-45T=	ENSP00000265134.6:n.478-45T=
ENST00000362057.3:c.1627-45T=	ENSP00000354623.3:n.1627-45T=
ENST00000374059.7:c.574-45T=	ENSP00000363172.3:n.574-45T=
NM_001083885.2:c.478-45T=	NP_001077354.2:n.478-45T=
NM_001173425.1:c.1627-45T=	NP_001166896.1:n.1627-45T=
NM_015404.3:c.1627-45T=	NP_056219.3:n.1627-45T=
XM_005251897.3:c.964-45T=	XP_005251954.2:n.964-45T=
XM_011518484.1:c.1660-45T=	XP_011516786.1:n.1660-45T=
XM_011518485.1:c.1660-45T=	XP_011516787.1:n.1660-45T=
XM_011518486.1:c.1660-45T=	XP_011516788.1:n.1660-45T=
XM_011518487.1:c.1534-45T=	XP_011516789.1:n.1534-45T=
XM_011518488.1:c.1417-45T=	XP_011516790.1:n.1417-45T=
XM_011518492.1:c.*12-45T=	XP_011516794.1:n.*12-45T=
XM_011518495.1:c.337-45T=	XP_011516797.1:n.337-45T=
XR_929747.1:n.2564-45T=
XR_929748.1:n.2462-45T=
XR_929750.1:n.2563-45T=
XR_929751.1:n.2470-45T=
XR_929757.1:n.2437-45T=
NM_001346890.1:c.574-45T=	NP_001333819.1:n.574-45T=
XM_011518486.2:c.1660-45T=	XP_011516788.1:n.1660-45T=
XM_011518487.2:c.1534-45T=	XP_011516789.1:n.1534-45T=
XM_011518488.2:c.1417-45T=	XP_011516790.1:n.1417-45T=
XM_011518492.2:c.*12-45T=	XP_011516794.1:n.*12-45T=
XR_929747.2:n.1875-45T=
XR_929748.2:n.1773-45T=
XR_929750.3:n.1874-45T=
XR_929757.2:n.1748-45T=
NM_015404.4:c.1627-45T= MANE Select	NP_056219.3:n.1627-45T=
NM_001173425.2:c.1627-45T=	NP_001166896.1:n.1627-45T=
NM_001083885.3:c.478-45T=	NP_001077354.2:n.478-45T=