Canonical Allele Identifier: CA2171795550

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472486C= , CM000677.2:g.40472486C=	GRCh38
NC_000015.9:g.40764685C= , CM000677.1:g.40764685C=	GRCh37
NC_000015.8:g.38551977C=	NCBI36
NG_017074.1:g.6526C= , LRG_600:g.6526C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*142C= MANE Select	ENSP00000307297.6:n.*142C=
ENST00000306243.6:c.*142C=	ENSP00000307297.5:n.*142C=
ENST00000559991.1:c.*142C=	ENSP00000453882.1:n.*142C=
NM_130468.3:c.*142C= , LRG_600t1:c.*142C=	NP_569735.1:n.*142C=
NM_130468.4:c.*142C= MANE Select	NP_569735.1:n.*142C=