Canonical Allele Identifier: CA383028961

Gene: SC5D

Linked Data

• gnomAD v4: 11-121307080-T-G
• MyVariant Identifiers: chr11:g.121177789T>G (hg19) ; chr11:g.121307080T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121307080T>G , CM000673.2:g.121307080T>G	GRCh38
NC_000011.9:g.121177789T>G , CM000673.1:g.121177789T>G	GRCh37
NC_000011.8:g.120682999T>G	NCBI36
NG_009446.1:g.19402T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264027.9:c.468T>G MANE Select	ENSP00000264027.4:p.Ile156Met
ENST00000264027.8:c.468T>G	ENSP00000264027.4:p.Ile156Met
ENST00000392789.2:c.468T>G	ENSP00000376539.2:p.Ile156Met
ENST00000527183.1:n.761T>G
ENST00000527762.5:c.489T>G	ENSP00000436290.1:p.Ile163Met
ENST00000528991.1:n.161T>G
ENST00000534230.5:c.468T>G	ENSP00000432550.1:p.Ile156Met
NM_001024956.2:c.468T>G	NP_001020127.1:p.Ile156Met
NM_006918.4:c.468T>G	NP_008849.2:p.Ile156Met
NM_006918.5:c.468T>G MANE Select	NP_008849.2:p.Ile156Met
NM_001024956.3:c.468T>G	NP_001020127.1:p.Ile156Met