Canonical Allele Identifier: CA1467353515

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71750923_71750929delinsCTTCTAA , CM000666.2:g.71750923_71750929delinsCTTCTAA	GRCh38
NC_000004.11:g.72616640_72616646delinsCTTCTAA , CM000666.1:g.72616640_72616646delinsCTTCTAA	GRCh37
NC_000004.10:g.72835504_72835510delinsCTTCTAA	NCBI36
NG_012837.2:g.59592_59598delinsTTAGAAG
NG_012837.3:g.59592_59598delinsTTAGAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.1395+1589_1395+1595delinsTTAGAAG MANE Select	ENSP00000273951.8:n.1395+1589_1395+1595delinsTTAGAAG
ENST00000273951.12:c.1395+1589_1395+1595delinsTTAGAAG	ENSP00000273951.8:n.1395+1589_1395+1595delinsTTAGAAG
ENST00000503364.5:n.68+3482_68+3488delinsTTAGAAG
ENST00000503472.5:n.1279+1589_1279+1595delinsTTAGAAG
ENST00000504199.5:c.1452+1589_1452+1595delinsTTAGAAG	ENSP00000421725.1:n.1452+1589_1452+1595delinsTTAGAAG
ENST00000509740.5:c.*218+1589_*218+1595delinsTTAGAAG	ENSP00000422664.1:n.*218+1589_*218+1595delinsTTAGAAG
ENST00000513476.5:c.1395+1589_1395+1595delinsTTAGAAG	ENSP00000426683.1:n.1395+1589_1395+1595delinsTTAGAAG
NM_000583.3:c.1395+1589_1395+1595delinsTTAGAAG	NP_000574.2:n.1395+1589_1395+1595delinsTTAGAAG
NM_001204306.1:c.1395+1589_1395+1595delinsTTAGAAG	NP_001191235.1:n.1395+1589_1395+1595delinsTTAGAAG
NM_001204307.1:c.1452+1589_1452+1595delinsTTAGAAG	NP_001191236.1:n.1452+1589_1452+1595delinsTTAGAAG
XM_006714177.2:c.1262+3482_1262+3488delinsTTAGAAG	XP_006714240.1:n.1262+3482_1262+3488delinsTTAGAAG
XM_006714177.3:c.1262+3482_1262+3488delinsTTAGAAG	XP_006714240.1:n.1262+3482_1262+3488delinsTTAGAAG
NM_000583.4:c.1395+1589_1395+1595delinsTTAGAAG MANE Select	NP_000574.2:n.1395+1589_1395+1595delinsTTAGAAG