Canonical Allele Identifier: CA2171795466

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472285G= , CM000677.2:g.40472285G=	GRCh38
NC_000015.9:g.40764484G= , CM000677.1:g.40764484G=	GRCh37
NC_000015.8:g.38551776G=	NCBI36
NG_017074.1:g.6325G= , LRG_600:g.6325G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.1072G= MANE Select	ENSP00000307297.6:p.Asp358=
ENST00000306243.6:c.1072G=	ENSP00000307297.5:p.Asp358=
ENST00000559991.1:c.997G=	ENSP00000453882.1:p.Asp333=
NM_130468.3:c.1072G= , LRG_600t1:c.1072G=	NP_569735.1:p.Asp358=
NM_130468.4:c.1072G= MANE Select	NP_569735.1:p.Asp358=