Canonical Allele Identifier: CA2171795567

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472528C= , CM000677.2:g.40472528C=	GRCh38
NC_000015.9:g.40764727C= , CM000677.1:g.40764727C=	GRCh37
NC_000015.8:g.38552019C=	NCBI36
NG_017074.1:g.6568C= , LRG_600:g.6568C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*184C= MANE Select	ENSP00000307297.6:n.*184C=
ENST00000306243.6:c.*184C=	ENSP00000307297.5:n.*184C=
ENST00000559991.1:c.*184C=	ENSP00000453882.1:n.*184C=
NM_130468.3:c.*184C= , LRG_600t1:c.*184C=	NP_569735.1:n.*184C=
NM_130468.4:c.*184C= MANE Select	NP_569735.1:n.*184C=