Canonical Allele Identifier: CA2616492243

Gene: SC5D

Linked Data

• gnomAD v4: 11-121303331-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121303331A>G , CM000673.2:g.121303331A>G	GRCh38
NC_000011.9:g.121174040A>G , CM000673.1:g.121174040A>G	GRCh37
NC_000011.8:g.120679250A>G	NCBI36
NG_009446.1:g.15653A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264027.9:c.-10-35A>G MANE Select	ENSP00000264027.4:n.-10-35A>G
ENST00000264027.8:c.-10-35A>G	ENSP00000264027.4:n.-10-35A>G
ENST00000392789.2:c.-10-35A>G	ENSP00000376539.2:n.-10-35A>G
ENST00000524683.5:n.47-35A>G
ENST00000527762.5:c.-10-35A>G	ENSP00000436290.1:n.-10-35A>G
ENST00000531140.1:n.59-35A>G
ENST00000534230.5:c.-10-35A>G	ENSP00000432550.1:n.-10-35A>G
ENST00000534455.5:n.137-35A>G
NM_001024956.2:c.-10-35A>G	NP_001020127.1:n.-10-35A>G
NM_006918.4:c.-10-35A>G	NP_008849.2:n.-10-35A>G
NM_006918.5:c.-10-35A>G MANE Select	NP_008849.2:n.-10-35A>G
NM_001024956.3:c.-10-35A>G	NP_001020127.1:n.-10-35A>G