Canonical Allele Identifier: CA2762138713

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756672_71756673insTTTTTTTT , CM000666.2:g.71756672_71756673insTTTTTTTT	GRCh38
NC_000004.11:g.72622389_72622390insTTTTTTTT , CM000666.1:g.72622389_72622390insTTTTTTTT	GRCh37
NC_000004.10:g.72841253_72841254insTTTTTTTT	NCBI36
NG_012837.2:g.53848_53849insAAAAAAAA
NG_012837.3:g.53848_53849insAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.1034+39_1034+40insAAAAAAAA MANE Select	ENSP00000273951.8:n.1034+39_1034+40insAAAAAAAA
ENST00000273951.12:c.1034+39_1034+40insAAAAAAAA	ENSP00000273951.8:n.1034+39_1034+40insAAAAAAAA
ENST00000503472.5:n.918+39_918+40insAAAAAAAA
ENST00000504199.5:c.1091+39_1091+40insAAAAAAAA	ENSP00000421725.1:n.1091+39_1091+40insAAAAAAAA
ENST00000509740.5:c.1034+39_1034+40insAAAAAAAA	ENSP00000422664.1:n.1034+39_1034+40insAAAAAAAA
ENST00000513476.5:c.1034+39_1034+40insAAAAAAAA	ENSP00000426683.1:n.1034+39_1034+40insAAAAAAAA
NM_000583.3:c.1034+39_1034+40insAAAAAAAA	NP_000574.2:n.1034+39_1034+40insAAAAAAAA
NM_001204306.1:c.1034+39_1034+40insAAAAAAAA	NP_001191235.1:n.1034+39_1034+40insAAAAAAAA
NM_001204307.1:c.1091+39_1091+40insAAAAAAAA	NP_001191236.1:n.1091+39_1091+40insAAAAAAAA
XM_006714177.2:c.1034+39_1034+40insAAAAAAAA	XP_006714240.1:n.1034+39_1034+40insAAAAAAAA
XM_006714177.3:c.1034+39_1034+40insAAAAAAAA	XP_006714240.1:n.1034+39_1034+40insAAAAAAAA
NM_000583.4:c.1034+39_1034+40insAAAAAAAA MANE Select	NP_000574.2:n.1034+39_1034+40insAAAAAAAA