Canonical Allele Identifier: CA2171795051

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40471378G= , CM000677.2:g.40471378G=	GRCh38
NC_000015.9:g.40763577G= , CM000677.1:g.40763577G=	GRCh37
NC_000015.8:g.38550869G=	NCBI36
NG_017074.1:g.5418G= , LRG_600:g.5418G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.165G= MANE Select	ENSP00000307297.6:p.Gly55=
ENST00000306243.6:c.165G=	ENSP00000307297.5:p.Gly55=
ENST00000559991.1:c.165G=	ENSP00000453882.1:p.Gly55=
NM_130468.3:c.165G= , LRG_600t1:c.165G=	NP_569735.1:p.Gly55=
NM_130468.4:c.165G= MANE Select	NP_569735.1:p.Gly55=