Canonical Allele Identifier: CA383028996

Gene: SC5D

Linked Data

• MyVariant Identifiers: chr11:g.121177792G>A (hg19) ; chr11:g.121307083G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121307083G>A , CM000673.2:g.121307083G>A	GRCh38
NC_000011.9:g.121177792G>A , CM000673.1:g.121177792G>A	GRCh37
NC_000011.8:g.120683002G>A	NCBI36
NG_009446.1:g.19405G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264027.9:c.471G>A MANE Select	ENSP00000264027.4:p.Trp157Ter
ENST00000264027.8:c.471G>A	ENSP00000264027.4:p.Trp157Ter
ENST00000392789.2:c.471G>A	ENSP00000376539.2:p.Trp157Ter
ENST00000527183.1:n.764G>A
ENST00000527762.5:c.492G>A	ENSP00000436290.1:p.Trp164Ter
ENST00000528991.1:n.164G>A
ENST00000534230.5:c.471G>A	ENSP00000432550.1:p.Trp157Ter
NM_001024956.2:c.471G>A	NP_001020127.1:p.Trp157Ter
NM_006918.4:c.471G>A	NP_008849.2:p.Trp157Ter
NM_006918.5:c.471G>A MANE Select	NP_008849.2:p.Trp157Ter
NM_001024956.3:c.471G>A	NP_001020127.1:p.Trp157Ter