Canonical Allele Identifier: CA1683126036

Gene: CHST12

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2408858T= , CM000669.2:g.2408858T=	GRCh38
NC_000007.13:g.2448493T= , CM000669.1:g.2448493T=	GRCh37
NC_000007.12:g.2415019T=	NCBI36
NG_029854.1:g.10299T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000618655.2:c.-78+5185T= MANE Select	ENSP00000481912.1:n.-78+5185T=
ENST00000258711.7:c.-78+5213T=	ENSP00000258711.6:n.-78+5213T=
ENST00000432336.1:c.-78+4652T=	ENSP00000411207.1:n.-78+4652T=
ENST00000618655.1:c.-78+5185T=	ENSP00000481912.1:n.-78+5185T=
NM_001243794.1:c.-78+5213T=	NP_001230723.1:n.-78+5213T=
NM_001243795.1:c.-78+5199T=	NP_001230724.1:n.-78+5199T=
NM_018641.4:c.-78+5185T=	NP_061111.1:n.-78+5185T=
XM_011515443.1:c.-78+4652T=	XP_011513745.1:n.-78+4652T=
XM_011515444.1:c.-78+5308T=	XP_011513746.1:n.-78+5308T=
XM_011515443.2:c.-78+4652T=	XP_011513745.1:n.-78+4652T=
XM_011515444.2:c.-78+5308T=	XP_011513746.1:n.-78+5308T=
NM_018641.5:c.-78+5185T= MANE Select	NP_061111.1:n.-78+5185T=
NM_001243794.2:c.-78+5213T=	NP_001230723.1:n.-78+5213T=
NM_001243795.2:c.-78+5199T=	NP_001230724.1:n.-78+5199T=