Canonical Allele Identifier: CA383026297

Gene: SC5D

Linked Data

• MyVariant Identifiers: chr11:g.121174231T>A (hg19) ; chr11:g.121303522T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121303522T>A , CM000673.2:g.121303522T>A	GRCh38
NC_000011.9:g.121174231T>A , CM000673.1:g.121174231T>A	GRCh37
NC_000011.8:g.120679441T>A	NCBI36
NG_009446.1:g.15844T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264027.9:c.147T>A MANE Select	ENSP00000264027.4:p.Cys49Ter
ENST00000264027.8:c.147T>A	ENSP00000264027.4:p.Cys49Ter
ENST00000392789.2:c.147T>A	ENSP00000376539.2:p.Cys49Ter
ENST00000524683.5:n.203T>A
ENST00000527762.5:c.147T>A	ENSP00000436290.1:p.Cys49Ter
ENST00000531140.1:n.215T>A
ENST00000534230.5:c.147T>A	ENSP00000432550.1:p.Cys49Ter
ENST00000534455.5:n.293T>A
NM_001024956.2:c.147T>A	NP_001020127.1:p.Cys49Ter
NM_006918.4:c.147T>A	NP_008849.2:p.Cys49Ter
NM_006918.5:c.147T>A MANE Select	NP_008849.2:p.Cys49Ter
NM_001024956.3:c.147T>A	NP_001020127.1:p.Cys49Ter