Canonical Allele Identifier: CA2171795056

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40471392T= , CM000677.2:g.40471392T=	GRCh38
NC_000015.9:g.40763591T= , CM000677.1:g.40763591T=	GRCh37
NC_000015.8:g.38550883T=	NCBI36
NG_017074.1:g.5432T= , LRG_600:g.5432T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.179T= MANE Select	ENSP00000307297.6:p.Ile60=
ENST00000306243.6:c.179T=	ENSP00000307297.5:p.Ile60=
ENST00000559991.1:c.179T=	ENSP00000453882.1:p.Ile60=
NM_130468.3:c.179T= , LRG_600t1:c.179T=	NP_569735.1:p.Ile60=
NM_130468.4:c.179T= MANE Select	NP_569735.1:p.Ile60=