Canonical Allele Identifier: CA1303181615

Gene: GCA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162350928_162350929delinsCT , CM000664.2:g.162350928_162350929delinsCT	GRCh38
NC_000002.11:g.163207438_163207439delinsCT , CM000664.1:g.163207438_163207439delinsCT	GRCh37
NC_000002.10:g.162915684_162915685delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000437150.7:c.193-1410_193-1409delinsCT MANE Select	ENSP00000394842.2:n.193-1410_193-1409delinsCT
ENST00000233612.8:c.136-1410_136-1409delinsCT	ENSP00000233612.4:n.136-1410_136-1409delinsCT
ENST00000429691.6:c.136-1410_136-1409delinsCT	ENSP00000412899.2:n.136-1410_136-1409delinsCT
ENST00000437150.6:c.193-1410_193-1409delinsCT	ENSP00000394842.2:n.193-1410_193-1409delinsCT
ENST00000446271.5:c.271-1410_271-1409delinsCT	ENSP00000393218.1:n.271-1410_271-1409delinsCT
ENST00000453113.6:c.136-1410_136-1409delinsCT	ENSP00000403805.2:n.136-1410_136-1409delinsCT
ENST00000473240.5:n.624-1410_624-1409delinsCT
ENST00000479199.1:n.260-1410_260-1409delinsCT
ENST00000481161.5:n.308-1410_308-1409delinsCT
ENST00000487445.6:n.283-1410_283-1409delinsCT
NM_012198.3:c.193-1410_193-1409delinsCT	NP_036330.1:n.193-1410_193-1409delinsCT
XM_005246446.2:c.193-1410_193-1409delinsCT	XP_005246503.1:n.193-1410_193-1409delinsCT
XM_006712398.2:c.271-1410_271-1409delinsCT	XP_006712461.1:n.271-1410_271-1409delinsCT
XM_006712399.2:c.271-1410_271-1409delinsCT	XP_006712462.1:n.271-1410_271-1409delinsCT
XM_006712400.2:c.238-1410_238-1409delinsCT	XP_006712463.1:n.238-1410_238-1409delinsCT
XM_006712401.2:c.271-1410_271-1409delinsCT	XP_006712464.1:n.271-1410_271-1409delinsCT
XM_011510926.1:c.136-1410_136-1409delinsCT	XP_011509228.1:n.136-1410_136-1409delinsCT
XM_011510927.1:c.136-1410_136-1409delinsCT	XP_011509229.1:n.136-1410_136-1409delinsCT
NM_001330265.1:c.238-1410_238-1409delinsCT	NP_001317194.1:n.238-1410_238-1409delinsCT
NM_001330266.1:c.238-1410_238-1409delinsCT	NP_001317195.1:n.238-1410_238-1409delinsCT
NM_001330267.1:c.238-1410_238-1409delinsCT	NP_001317196.1:n.238-1410_238-1409delinsCT
NM_001330268.1:c.271-1410_271-1409delinsCT	NP_001317197.1:n.271-1410_271-1409delinsCT
NM_001330270.1:c.136-1410_136-1409delinsCT	NP_001317199.1:n.136-1410_136-1409delinsCT
NM_001330271.1:c.136-1410_136-1409delinsCT	NP_001317200.1:n.136-1410_136-1409delinsCT
NM_012198.4:c.193-1410_193-1409delinsCT	NP_036330.1:n.193-1410_193-1409delinsCT
XM_005246446.3:c.193-1410_193-1409delinsCT	XP_005246503.1:n.193-1410_193-1409delinsCT
XM_006712398.4:c.271-1410_271-1409delinsCT	XP_006712461.1:n.271-1410_271-1409delinsCT
XM_006712400.4:c.238-1410_238-1409delinsCT	XP_006712463.1:n.238-1410_238-1409delinsCT
XM_011510926.2:c.136-1410_136-1409delinsCT	XP_011509228.1:n.136-1410_136-1409delinsCT
XM_017003767.1:c.136-1410_136-1409delinsCT	XP_016859256.1:n.136-1410_136-1409delinsCT
XM_017003769.2:c.271-1410_271-1409delinsCT	XP_016859258.1:n.271-1410_271-1409delinsCT
NM_012198.5:c.193-1410_193-1409delinsCT MANE Select	NP_036330.1:n.193-1410_193-1409delinsCT
NM_001330270.2:c.136-1410_136-1409delinsCT	NP_001317199.1:n.136-1410_136-1409delinsCT
NM_001330271.2:c.136-1410_136-1409delinsCT	NP_001317200.1:n.136-1410_136-1409delinsCT