Canonical Allele Identifier: CA383029275

Gene: SC5D

Linked Data

• MyVariant Identifiers: chr11:g.121177823T>G (hg19) ; chr11:g.121307114T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121307114T>G , CM000673.2:g.121307114T>G	GRCh38
NC_000011.9:g.121177823T>G , CM000673.1:g.121177823T>G	GRCh37
NC_000011.8:g.120683033T>G	NCBI36
NG_009446.1:g.19436T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264027.9:c.502T>G MANE Select	ENSP00000264027.4:p.Phe168Val
ENST00000264027.8:c.502T>G	ENSP00000264027.4:p.Phe168Val
ENST00000392789.2:c.502T>G	ENSP00000376539.2:p.Phe168Val
ENST00000527183.1:n.795T>G
ENST00000527762.5:c.523T>G	ENSP00000436290.1:p.Phe175Val
ENST00000528991.1:n.195T>G
ENST00000534230.5:c.502T>G	ENSP00000432550.1:p.Phe168Val
NM_001024956.2:c.502T>G	NP_001020127.1:p.Phe168Val
NM_006918.4:c.502T>G	NP_008849.2:p.Phe168Val
NM_006918.5:c.502T>G MANE Select	NP_008849.2:p.Phe168Val
NM_001024956.3:c.502T>G	NP_001020127.1:p.Phe168Val