Canonical Allele Identifier: CA2171795586

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472557G= , CM000677.2:g.40472557G=	GRCh38
NC_000015.9:g.40764756G= , CM000677.1:g.40764756G=	GRCh37
NC_000015.8:g.38552048G=	NCBI36
NG_017074.1:g.6597G= , LRG_600:g.6597G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*213G= MANE Select	ENSP00000307297.6:n.*213G=
ENST00000306243.6:c.*213G=	ENSP00000307297.5:n.*213G=
ENST00000559991.1:c.*213G=	ENSP00000453882.1:n.*213G=
NM_130468.3:c.*213G= , LRG_600t1:c.*213G=	NP_569735.1:n.*213G=
NM_130468.4:c.*213G= MANE Select	NP_569735.1:n.*213G=