Canonical Allele Identifier: CA2004810379

Gene: SC5D

Linked Data

• dbSNP Id: rs1947969395

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121306837_121306843del , CM000673.2:g.121306837_121306843del	GRCh38
NC_000011.9:g.121177546_121177552del , CM000673.1:g.121177546_121177552del	GRCh37
NC_000011.8:g.120682756_120682762del	NCBI36
NG_009446.1:g.19159_19165del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264027.9:c.445-220_445-214del MANE Select	ENSP00000264027.4:n.445-220_445-214del
ENST00000264027.8:c.445-220_445-214del	ENSP00000264027.4:n.445-220_445-214del
ENST00000392789.2:c.445-220_445-214del	ENSP00000376539.2:n.445-220_445-214del
ENST00000527183.1:n.738-220_738-214del
ENST00000527762.5:c.466-220_466-214del	ENSP00000436290.1:n.466-220_466-214del
ENST00000528991.1:n.138-220_138-214del
ENST00000534230.5:c.445-220_445-214del	ENSP00000432550.1:n.445-220_445-214del
NM_001024956.2:c.445-220_445-214del	NP_001020127.1:n.445-220_445-214del
NM_006918.4:c.445-220_445-214del	NP_008849.2:n.445-220_445-214del
NM_006918.5:c.445-220_445-214del MANE Select	NP_008849.2:n.445-220_445-214del
NM_001024956.3:c.445-220_445-214del	NP_001020127.1:n.445-220_445-214del