Canonical Allele Identifier: CA2171795354

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472000T= , CM000677.2:g.40472000T=	GRCh38
NC_000015.9:g.40764199T= , CM000677.1:g.40764199T=	GRCh37
NC_000015.8:g.38551491T=	NCBI36
NG_017074.1:g.6040T= , LRG_600:g.6040T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000306243.7:c.787T= MANE Select	ENSP00000307297.6:p.Phe263=
ENST00000306243.6:c.787T=	ENSP00000307297.5:p.Phe263=
ENST00000559991.1:c.712T=	ENSP00000453882.1:p.Phe238=
NM_130468.3:c.787T= , LRG_600t1:c.787T=	NP_569735.1:p.Phe263=
NM_130468.4:c.787T= MANE Select	NP_569735.1:p.Phe263=