Canonical Allele Identifier: CA1064015982

Gene: GC

Linked Data

• dbSNP Id: rs1741254799
• gnomAD v3: 4-71743506-ACT-A
• gnomAD v4: 4-71743506-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71743508_71743509del , CM000666.2:g.71743508_71743509del	GRCh38
NC_000004.11:g.72609225_72609226del , CM000666.1:g.72609225_72609226del	GRCh37
NC_000004.10:g.72828089_72828090del	NCBI36
NG_012837.2:g.67013_67014del
NG_012837.3:g.67013_67014del

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.*26-1638_*26-1637del MANE Select	ENSP00000273951.8:n.*26-1638_*26-1637del
ENST00000273951.12:c.*26-1638_*26-1637del	ENSP00000273951.8:n.*26-1638_*26-1637del
ENST00000503364.5:n.124-1638_124-1637del
ENST00000503472.5:n.1335-1638_1335-1637del
ENST00000504199.5:c.*26-1638_*26-1637del	ENSP00000421725.1:n.*26-1638_*26-1637del
ENST00000509740.5:c.*274-1638_*274-1637del	ENSP00000422664.1:n.*274-1638_*274-1637de...
ENST00000513476.5:c.1396-1638_1396-1637del	ENSP00000426683.1:n.1396-1638_1396-1637de...
NM_000583.3:c.*26-1638_*26-1637del	NP_000574.2:n.*26-1638_*26-1637del
NM_001204306.1:c.*26-1638_*26-1637del	NP_001191235.1:n.*26-1638_*26-1637del
NM_001204307.1:c.*26-1638_*26-1637del	NP_001191236.1:n.*26-1638_*26-1637del
XM_006714177.2:c.*40-1638_*40-1637del	XP_006714240.1:n.*40-1638_*40-1637del
XM_006714177.3:c.*40-1638_*40-1637del	XP_006714240.1:n.*40-1638_*40-1637del
NM_000583.4:c.*26-1638_*26-1637del MANE Select	NP_000574.2:n.*26-1638_*26-1637del