Canonical Allele Identifier: CA1467350225

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71743724_71743725delinsCT , CM000666.2:g.71743724_71743725delinsCT	GRCh38
NC_000004.11:g.72609441_72609442delinsCT , CM000666.1:g.72609441_72609442delinsCT	GRCh37
NC_000004.10:g.72828305_72828306delinsCT	NCBI36
NG_012837.2:g.66796_66797delinsAG
NG_012837.3:g.66796_66797delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.*26-1855_*26-1854delinsAG MANE Select	ENSP00000273951.8:n.*26-1855_*26-1854deli...
ENST00000273951.12:c.*26-1855_*26-1854delinsAG	ENSP00000273951.8:n.*26-1855_*26-1854deli...
ENST00000503364.5:n.124-1855_124-1854delinsAG
ENST00000503472.5:n.1335-1855_1335-1854delinsAG
ENST00000504199.5:c.*26-1855_*26-1854delinsAG	ENSP00000421725.1:n.*26-1855_*26-1854deli...
ENST00000509740.5:c.*274-1855_*274-1854delinsAG	ENSP00000422664.1:n.*274-1855_*274-1854de...
ENST00000513476.5:c.1396-1855_1396-1854delinsAG	ENSP00000426683.1:n.1396-1855_1396-1854de...
NM_000583.3:c.*26-1855_*26-1854delinsAG	NP_000574.2:n.*26-1855_*26-1854delinsAG
NM_001204306.1:c.*26-1855_*26-1854delinsAG	NP_001191235.1:n.*26-1855_*26-1854delinsA...
NM_001204307.1:c.*26-1855_*26-1854delinsAG	NP_001191236.1:n.*26-1855_*26-1854delinsA...
XM_006714177.2:c.*40-1855_*40-1854delinsAG	XP_006714240.1:n.*40-1855_*40-1854delinsA...
XM_006714177.3:c.*40-1855_*40-1854delinsAG	XP_006714240.1:n.*40-1855_*40-1854delinsA...
NM_000583.4:c.*26-1855_*26-1854delinsAG MANE Select	NP_000574.2:n.*26-1855_*26-1854delinsAG