Canonical Allele Identifier: CA2171795555

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472496G= , CM000677.2:g.40472496G=	GRCh38
NC_000015.9:g.40764695G= , CM000677.1:g.40764695G=	GRCh37
NC_000015.8:g.38551987G=	NCBI36
NG_017074.1:g.6536G= , LRG_600:g.6536G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*152G= MANE Select	ENSP00000307297.6:n.*152G=
ENST00000306243.6:c.*152G=	ENSP00000307297.5:n.*152G=
ENST00000559991.1:c.*152G=	ENSP00000453882.1:n.*152G=
NM_130468.3:c.*152G= , LRG_600t1:c.*152G=	NP_569735.1:n.*152G=
NM_130468.4:c.*152G= MANE Select	NP_569735.1:n.*152G=