Canonical Allele Identifier: CA1467380583

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71773018_71773019delinsTG , CM000666.2:g.71773018_71773019delinsTG	GRCh38
NC_000004.11:g.72638735_72638736delinsTG , CM000666.1:g.72638735_72638736delinsTG	GRCh37
NC_000004.10:g.72857599_72857600delinsTG	NCBI36
NG_012837.2:g.37502_37503delinsCA
NG_012837.3:g.37502_37503delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.59-3619_59-3618delinsCA MANE Select	ENSP00000273951.8:n.59-3619_59-3618delins...
ENST00000273951.12:c.59-3619_59-3618delinsCA	ENSP00000273951.8:n.59-3619_59-3618delins...
ENST00000504199.5:c.116-3619_116-3618delinsCA	ENSP00000421725.1:n.116-3619_116-3618deli...
ENST00000506245.1:c.59-3619_59-3618delinsCA	ENSP00000426718.1:n.59-3619_59-3618delins...
ENST00000509740.5:c.59-3619_59-3618delinsCA	ENSP00000422664.1:n.59-3619_59-3618delins...
ENST00000513476.5:c.59-3619_59-3618delinsCA	ENSP00000426683.1:n.59-3619_59-3618delins...
NM_000583.3:c.59-3619_59-3618delinsCA	NP_000574.2:n.59-3619_59-3618delinsCA
NM_001204306.1:c.59-3619_59-3618delinsCA	NP_001191235.1:n.59-3619_59-3618delinsCA
NM_001204307.1:c.116-3619_116-3618delinsCA	NP_001191236.1:n.116-3619_116-3618delinsC...
XM_006714177.2:c.59-3619_59-3618delinsCA	XP_006714240.1:n.59-3619_59-3618delinsCA
XM_006714177.3:c.59-3619_59-3618delinsCA	XP_006714240.1:n.59-3619_59-3618delinsCA
NM_000583.4:c.59-3619_59-3618delinsCA MANE Select	NP_000574.2:n.59-3619_59-3618delinsCA