Canonical Allele Identifier: CA477217293

Gene: SC5D

Linked Data

• MyVariant Identifiers: chr11:g.121174135G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121303426G>T , CM000673.2:g.121303426G>T	GRCh38
NC_000011.9:g.121174135G>T , CM000673.1:g.121174135G>T	GRCh37
NC_000011.8:g.120679345G>T	NCBI36
NG_009446.1:g.15748G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264027.9:c.51G>T MANE Select	ENSP00000264027.4:p.Val17=
ENST00000264027.8:c.51G>T	ENSP00000264027.4:p.Val17=
ENST00000392789.2:c.51G>T	ENSP00000376539.2:p.Val17=
ENST00000524683.5:n.107G>T
ENST00000527762.5:c.51G>T	ENSP00000436290.1:p.Val17=
ENST00000531140.1:n.119G>T
ENST00000534230.5:c.51G>T	ENSP00000432550.1:p.Val17=
ENST00000534455.5:n.197G>T
NM_001024956.2:c.51G>T	NP_001020127.1:p.Val17=
NM_006918.4:c.51G>T	NP_008849.2:p.Val17=
NM_006918.5:c.51G>T MANE Select	NP_008849.2:p.Val17=
NM_001024956.3:c.51G>T	NP_001020127.1:p.Val17=