Canonical Allele Identifier: CA477217398
Gene: SC5D HGNC NCBI

Linked Data

dbSNP Id: rs1947940697
MyVariant Identifiers: chr11:g.121174228C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121303519C>T , CM000673.2:g.121303519C>T GRCh38
NC_000011.9:g.121174228C>T , CM000673.1:g.121174228C>T GRCh37
NC_000011.8:g.120679438C>T NCBI36
NG_009446.1:g.15841C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264027.9:c.144C>T MANE Select ENSP00000264027.4:p.Phe48=
ENST00000264027.8:c.144C>T ENSP00000264027.4:p.Phe48=
ENST00000392789.2:c.144C>T ENSP00000376539.2:p.Phe48=
ENST00000524683.5:n.200C>T
ENST00000527762.5:c.144C>T ENSP00000436290.1:p.Phe48=
ENST00000531140.1:n.212C>T
ENST00000534230.5:c.144C>T ENSP00000432550.1:p.Phe48=
ENST00000534455.5:n.290C>T
NM_001024956.2:c.144C>T NP_001020127.1:p.Phe48=
NM_006918.4:c.144C>T NP_008849.2:p.Phe48=
NM_006918.5:c.144C>T MANE Select NP_008849.2:p.Phe48=
NM_001024956.3:c.144C>T NP_001020127.1:p.Phe48=