Canonical Allele Identifier: CA1063999690

Gene: GC

Linked Data

• dbSNP Id: rs1161195179
• gnomAD v3: 4-71777775-TA-T
• gnomAD v4: 4-71777775-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71777782del , CM000666.2:g.71777782del	GRCh38
NC_000004.11:g.72643499del , CM000666.1:g.72643499del	GRCh37
NC_000004.10:g.72862363del	NCBI36
NG_012837.2:g.32745del
NG_012837.3:g.32745del

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.58+6185del MANE Select	ENSP00000273951.8:n.58+6185del
ENST00000273951.12:c.58+6185del	ENSP00000273951.8:n.58+6185del
ENST00000504199.5:c.115+6185del	ENSP00000421725.1:n.115+6185del
ENST00000506245.1:c.58+6185del	ENSP00000426718.1:n.58+6185del
ENST00000509740.5:c.58+6185del	ENSP00000422664.1:n.58+6185del
ENST00000513476.5:c.58+6185del	ENSP00000426683.1:n.58+6185del
NM_000583.3:c.58+6185del	NP_000574.2:n.58+6185del
NM_001204306.1:c.58+6185del	NP_001191235.1:n.58+6185del
NM_001204307.1:c.115+6185del	NP_001191236.1:n.115+6185del
XM_006714177.2:c.58+6185del	XP_006714240.1:n.58+6185del
XM_006714177.3:c.58+6185del	XP_006714240.1:n.58+6185del
NM_000583.4:c.58+6185del MANE Select	NP_000574.2:n.58+6185del