Canonical Allele Identifier: CA2171795467

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472292C= , CM000677.2:g.40472292C=	GRCh38
NC_000015.9:g.40764491C= , CM000677.1:g.40764491C=	GRCh37
NC_000015.8:g.38551783C=	NCBI36
NG_017074.1:g.6332C= , LRG_600:g.6332C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.1079C= MANE Select	ENSP00000307297.6:p.Ser360=
ENST00000306243.6:c.1079C=	ENSP00000307297.5:p.Ser360=
ENST00000559991.1:c.1004C=	ENSP00000453882.1:p.Ser335=
NM_130468.3:c.1079C= , LRG_600t1:c.1079C=	NP_569735.1:p.Ser360=
NM_130468.4:c.1079C= MANE Select	NP_569735.1:p.Ser360=