Canonical Allele Identifier: CA2171794929

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40471185C= , CM000677.2:g.40471185C=	GRCh38
NC_000015.9:g.40763384C= , CM000677.1:g.40763384C=	GRCh37
NC_000015.8:g.38550676C=	NCBI36
NG_017074.1:g.5225C= , LRG_600:g.5225C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.-29C= MANE Select	ENSP00000307297.6:n.-29C=
ENST00000306243.6:c.-29C=	ENSP00000307297.5:n.-29C=
ENST00000559991.1:c.-29C=	ENSP00000453882.1:n.-29C=
NM_130468.3:c.-29C= , LRG_600t1:c.-29C=	NP_569735.1:n.-29C=
NM_130468.4:c.-29C= MANE Select	NP_569735.1:n.-29C=