Canonical Allele Identifier: CA2171794918

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40471171T= , CM000677.2:g.40471171T=	GRCh38
NC_000015.9:g.40763370T= , CM000677.1:g.40763370T=	GRCh37
NC_000015.8:g.38550662T=	NCBI36
NG_017074.1:g.5211T= , LRG_600:g.5211T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.-43T= MANE Select	ENSP00000307297.6:n.-43T=
ENST00000306243.6:c.-43T=	ENSP00000307297.5:n.-43T=
ENST00000559991.1:c.-43T=	ENSP00000453882.1:n.-43T=
NM_130468.3:c.-43T= , LRG_600t1:c.-43T=	NP_569735.1:n.-43T=
NM_130468.4:c.-43T= MANE Select	NP_569735.1:n.-43T=