Canonical Allele Identifier: CA1873825795

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114403844C= , CM000671.2:g.114403844C=	GRCh38
NC_000009.11:g.117166124C= , CM000671.1:g.117166124C=	GRCh37
NC_000009.10:g.116205945C=	NCBI36
NG_016700.1:g.106613G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.762+52G=	ENSP00000514396.1:n.762+52G=
ENST00000362057.4:c.2418+52G= MANE Select	ENSP00000354623.3:n.2418+52G=
ENST00000674036.8:c.1391+52G=
ENST00000674048.1:n.2299+52G=
ENST00000265134.10:c.1269+52G=	ENSP00000265134.6:n.1269+52G=
ENST00000362057.3:c.2418+52G=	ENSP00000354623.3:n.2418+52G=
ENST00000374059.7:c.1365+52G=	ENSP00000363172.3:n.1365+52G=
NM_001083885.2:c.1269+52G=	NP_001077354.2:n.1269+52G=
NM_001173425.1:c.2415+52G=	NP_001166896.1:n.2415+52G=
NM_015404.3:c.2418+52G=	NP_056219.3:n.2418+52G=
XM_005251897.3:c.1755+52G=	XP_005251954.2:n.1755+52G=
XM_011518484.1:c.2451+52G=	XP_011516786.1:n.2451+52G=
XM_011518485.1:c.2451+52G=	XP_011516787.1:n.2451+52G=
XM_011518486.1:c.2448+52G=	XP_011516788.1:n.2448+52G=
XM_011518487.1:c.2325+52G=	XP_011516789.1:n.2325+52G=
XM_011518488.1:c.2208+52G=	XP_011516790.1:n.2208+52G=
XM_011518495.1:c.1128+52G=	XP_011516797.1:n.1128+52G=
XR_929747.1:n.3355+52G=
XR_929748.1:n.3253+52G=
NM_001346890.1:c.1365+52G=	NP_001333819.1:n.1365+52G=
XM_011518486.2:c.2448+52G=	XP_011516788.1:n.2448+52G=
XM_011518487.2:c.2325+52G=	XP_011516789.1:n.2325+52G=
XM_011518488.2:c.2208+52G=	XP_011516790.1:n.2208+52G=
XR_929747.2:n.2666+52G=
XR_929748.2:n.2564+52G=
NM_015404.4:c.2418+52G= MANE Select	NP_056219.3:n.2418+52G=
NM_001173425.2:c.2415+52G=	NP_001166896.1:n.2415+52G=
NM_001083885.3:c.1269+52G=	NP_001077354.2:n.1269+52G=