Canonical Allele Identifier: CA2171795001

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40471292C= , CM000677.2:g.40471292C=	GRCh38
NC_000015.9:g.40763491C= , CM000677.1:g.40763491C=	GRCh37
NC_000015.8:g.38550783C=	NCBI36
NG_017074.1:g.5332C= , LRG_600:g.5332C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000306243.7:c.79C= MANE Select	ENSP00000307297.6:p.Leu27=
ENST00000306243.6:c.79C=	ENSP00000307297.5:p.Leu27=
ENST00000559991.1:c.79C=	ENSP00000453882.1:p.Leu27=
NM_130468.3:c.79C= , LRG_600t1:c.79C=	NP_569735.1:p.Leu27=
NM_130468.4:c.79C= MANE Select	NP_569735.1:p.Leu27=