Canonical Allele Identifier: CA1873825360

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402847G= , CM000671.2:g.114402847G=	GRCh38
NC_000009.11:g.117165127G= , CM000671.1:g.117165127G=	GRCh37
NC_000009.10:g.116204948G=	NCBI36
NG_016700.1:g.107610C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.975C=	ENSP00000514396.1:p.His325=
ENST00000362057.4:c.2631C= MANE Select	ENSP00000354623.3:p.His877=
ENST00000674036.8:c.1604C=
ENST00000674048.1:n.2512C=
ENST00000265134.10:c.1482C=	ENSP00000265134.6:p.His494=
ENST00000362057.3:c.2631C=	ENSP00000354623.3:p.His877=
ENST00000374059.7:c.1578C=	ENSP00000363172.3:p.His526=
NM_001083885.2:c.1482C=	NP_001077354.2:p.His494=
NM_001173425.1:c.2628C=	NP_001166896.1:p.His876=
NM_015404.3:c.2631C=	NP_056219.3:p.His877=
XM_005251897.3:c.1968C=	XP_005251954.2:p.His656=
XM_011518484.1:c.2664C=	XP_011516786.1:p.His888=
XM_011518485.1:c.2664C=	XP_011516787.1:p.His888=
XM_011518486.1:c.2661C=	XP_011516788.1:p.His887=
XM_011518487.1:c.2538C=	XP_011516789.1:p.His846=
XM_011518488.1:c.2421C=	XP_011516790.1:p.His807=
XM_011518495.1:c.1341C=	XP_011516797.1:p.His447=
NM_001346890.1:c.1578C=	NP_001333819.1:p.His526=
XM_011518486.2:c.2661C=	XP_011516788.1:p.His887=
XM_011518487.2:c.2538C=	XP_011516789.1:p.His846=
XM_011518488.2:c.2421C=	XP_011516790.1:p.His807=
NM_015404.4:c.2631C= MANE Select	NP_056219.3:p.His877=
NM_001173425.2:c.2628C=	NP_001166896.1:p.His876=
NM_001083885.3:c.1482C=	NP_001077354.2:p.His494=