Canonical Allele Identifier: CA2171794999

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40471290C= , CM000677.2:g.40471290C=	GRCh38
NC_000015.9:g.40763489C= , CM000677.1:g.40763489C=	GRCh37
NC_000015.8:g.38550781C=	NCBI36
NG_017074.1:g.5330C= , LRG_600:g.5330C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000306243.7:c.77C= MANE Select	ENSP00000307297.6:p.Pro26=
ENST00000306243.6:c.77C=	ENSP00000307297.5:p.Pro26=
ENST00000559991.1:c.77C=	ENSP00000453882.1:p.Pro26=
NM_130468.3:c.77C= , LRG_600t1:c.77C=	NP_569735.1:p.Pro26=
NM_130468.4:c.77C= MANE Select	NP_569735.1:p.Pro26=