Canonical Allele Identifier: CA477383690

Gene: SC5D

Linked Data

• MyVariant Identifiers: chr11:g.121177813A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121307104A>T , CM000673.2:g.121307104A>T	GRCh38
NC_000011.9:g.121177813A>T , CM000673.1:g.121177813A>T	GRCh37
NC_000011.8:g.120683023A>T	NCBI36
NG_009446.1:g.19426A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264027.9:c.492A>T MANE Select	ENSP00000264027.4:p.Ala164=
ENST00000264027.8:c.492A>T	ENSP00000264027.4:p.Ala164=
ENST00000392789.2:c.492A>T	ENSP00000376539.2:p.Ala164=
ENST00000527183.1:n.785A>T
ENST00000527762.5:c.513A>T	ENSP00000436290.1:p.Ala171=
ENST00000528991.1:n.185A>T
ENST00000534230.5:c.492A>T	ENSP00000432550.1:p.Ala164=
NM_001024956.2:c.492A>T	NP_001020127.1:p.Ala164=
NM_006918.4:c.492A>T	NP_008849.2:p.Ala164=
NM_006918.5:c.492A>T MANE Select	NP_008849.2:p.Ala164=
NM_001024956.3:c.492A>T	NP_001020127.1:p.Ala164=