Canonical Allele Identifier: CA2171795039

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40471361A= , CM000677.2:g.40471361A=	GRCh38
NC_000015.9:g.40763560A= , CM000677.1:g.40763560A=	GRCh37
NC_000015.8:g.38550852A=	NCBI36
NG_017074.1:g.5401A= , LRG_600:g.5401A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.148A= MANE Select	ENSP00000307297.6:p.Ile50=
ENST00000306243.6:c.148A=	ENSP00000307297.5:p.Ile50=
ENST00000559991.1:c.148A=	ENSP00000453882.1:p.Ile50=
NM_130468.3:c.148A= , LRG_600t1:c.148A=	NP_569735.1:p.Ile50=
NM_130468.4:c.148A= MANE Select	NP_569735.1:p.Ile50=