Canonical Allele Identifier: CA1467353665

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71751304_71751308delinsTAACA , CM000666.2:g.71751304_71751308delinsTAACA	GRCh38
NC_000004.11:g.72617021_72617025delinsTAACA , CM000666.1:g.72617021_72617025delinsTAACA	GRCh37
NC_000004.10:g.72835885_72835889delinsTAACA	NCBI36
NG_012837.2:g.59213_59217delinsTGTTA
NG_012837.3:g.59213_59217delinsTGTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.1395+1210_1395+1214delinsTGTTA MANE Select	ENSP00000273951.8:n.1395+1210_1395+1214de...
ENST00000273951.12:c.1395+1210_1395+1214delinsTGTTA	ENSP00000273951.8:n.1395+1210_1395+1214de...
ENST00000503364.5:n.68+3103_68+3107delinsTGTTA
ENST00000503472.5:n.1279+1210_1279+1214delinsTGTTA
ENST00000504199.5:c.1452+1210_1452+1214delinsTGTTA	ENSP00000421725.1:n.1452+1210_1452+1214de...
ENST00000509740.5:c.*218+1210_*218+1214delinsTGTTA	ENSP00000422664.1:n.*218+1210_*218+1214de...
ENST00000513476.5:c.1395+1210_1395+1214delinsTGTTA	ENSP00000426683.1:n.1395+1210_1395+1214de...
NM_000583.3:c.1395+1210_1395+1214delinsTGTTA	NP_000574.2:n.1395+1210_1395+1214delinsTG...
NM_001204306.1:c.1395+1210_1395+1214delinsTGTTA	NP_001191235.1:n.1395+1210_1395+1214delin...
NM_001204307.1:c.1452+1210_1452+1214delinsTGTTA	NP_001191236.1:n.1452+1210_1452+1214delin...
XM_006714177.2:c.1262+3103_1262+3107delinsTGTTA	XP_006714240.1:n.1262+3103_1262+3107delin...
XM_006714177.3:c.1262+3103_1262+3107delinsTGTTA	XP_006714240.1:n.1262+3103_1262+3107delin...
NM_000583.4:c.1395+1210_1395+1214delinsTGTTA MANE Select	NP_000574.2:n.1395+1210_1395+1214delinsTG...