Canonical Allele Identifier: CA2171795394

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472097T= , CM000677.2:g.40472097T=	GRCh38
NC_000015.9:g.40764296T= , CM000677.1:g.40764296T=	GRCh37
NC_000015.8:g.38551588T=	NCBI36
NG_017074.1:g.6137T= , LRG_600:g.6137T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000306243.7:c.884T= MANE Select	ENSP00000307297.6:p.Phe295=
ENST00000306243.6:c.884T=	ENSP00000307297.5:p.Phe295=
ENST00000559991.1:c.809T=	ENSP00000453882.1:p.Phe270=
NM_130468.3:c.884T= , LRG_600t1:c.884T=	NP_569735.1:p.Phe295=
NM_130468.4:c.884T= MANE Select	NP_569735.1:p.Phe295=