Canonical Allele Identifier: CA2171795469

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472294C= , CM000677.2:g.40472294C=	GRCh38
NC_000015.9:g.40764493C= , CM000677.1:g.40764493C=	GRCh37
NC_000015.8:g.38551785C=	NCBI36
NG_017074.1:g.6334C= , LRG_600:g.6334C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.1081C= MANE Select	ENSP00000307297.6:p.Leu361=
ENST00000306243.6:c.1081C=	ENSP00000307297.5:p.Leu361=
ENST00000559991.1:c.1006C=	ENSP00000453882.1:p.Leu336=
NM_130468.3:c.1081C= , LRG_600t1:c.1081C=	NP_569735.1:p.Leu361=
NM_130468.4:c.1081C= MANE Select	NP_569735.1:p.Leu361=