Canonical Allele Identifier: CA2171795573

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472539A= , CM000677.2:g.40472539A=	GRCh38
NC_000015.9:g.40764738A= , CM000677.1:g.40764738A=	GRCh37
NC_000015.8:g.38552030A=	NCBI36
NG_017074.1:g.6579A= , LRG_600:g.6579A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*195A= MANE Select	ENSP00000307297.6:n.*195A=
ENST00000306243.6:c.*195A=	ENSP00000307297.5:n.*195A=
ENST00000559991.1:c.*195A=	ENSP00000453882.1:n.*195A=
NM_130468.3:c.*195A= , LRG_600t1:c.*195A=	NP_569735.1:n.*195A=
NM_130468.4:c.*195A= MANE Select	NP_569735.1:n.*195A=