Canonical Allele Identifier: CA552292685

Gene: GC

Linked Data

• dbSNP Id: rs1560710348
• gnomAD v2: 4-72649785-T-TTTACAGGAATTCTTACTA
• MyVariant Identifiers: chr4:g.72649785_72649786insTTACAGGAATTCTTACTA (hg19) ; chr4:g.71784068_71784069insTTACAGGAATTCTTACTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71784068_71784069insTTACAGGAATTCTTACTA , CM000666.2:g.71784068_71784069insTTACAGGAATTCTTACTA	GRCh38
NC_000004.11:g.72649785_72649786insTTACAGGAATTCTTACTA , CM000666.1:g.72649785_72649786insTTACAGGAATTCTTACTA	GRCh37
NC_000004.10:g.72868649_72868650insTTACAGGAATTCTTACTA	NCBI36
NG_012837.2:g.26452_26453insTAGTAAGAATTCCTGTAA
NG_012837.3:g.26452_26453insTAGTAAGAATTCCTGTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.-51_-50insTAGTAAGAATTCCTGTAA MANE Select	ENSP00000273951.8:n.-51_-50insTAGTAAGAATTCCTGTAA
ENST00000273951.12:c.-51_-50insTAGTAAGAATTCCTGTAA	ENSP00000273951.8:n.-51_-50insTAGTAAGAATTCCTGTAA
ENST00000504199.5:c.22-15_22-14insTAGTAAGAATTCCTGTAA	ENSP00000421725.1:n.22-15_22-14insTAGTAAGAATTCCTGTAA
ENST00000506245.1:c.-36-15_-36-14insTAGTAAGAATTCCTGTAA	ENSP00000426718.1:n.-36-15_-36-14insTAGTAAGAATTCCTGTAA
NM_000583.3:c.-51_-50insTAGTAAGAATTCCTGTAA	NP_000574.2:n.-51_-50insTAGTAAGAATTCCTGTAA
NM_001204306.1:c.-36-15_-36-14insTAGTAAGAATTCCTGTAA	NP_001191235.1:n.-36-15_-36-14insTAGTAAGAATTCCTGTAA
NM_001204307.1:c.22-15_22-14insTAGTAAGAATTCCTGTAA	NP_001191236.1:n.22-15_22-14insTAGTAAGAATTCCTGTAA
XM_006714177.2:c.-51_-50insTAGTAAGAATTCCTGTAA	XP_006714240.1:n.-51_-50insTAGTAAGAATTCCTGTAA
XM_006714177.3:c.-51_-50insTAGTAAGAATTCCTGTAA	XP_006714240.1:n.-51_-50insTAGTAAGAATTCCTGTAA
NM_000583.4:c.-51_-50insTAGTAAGAATTCCTGTAA MANE Select	NP_000574.2:n.-51_-50insTAGTAAGAATTCCTGTAA