Canonical Allele Identifier: CA1303181636

Gene: GCA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162350988_162350989delinsAC , CM000664.2:g.162350988_162350989delinsAC	GRCh38
NC_000002.11:g.163207498_163207499delinsAC , CM000664.1:g.163207498_163207499delinsAC	GRCh37
NC_000002.10:g.162915744_162915745delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437150.7:c.193-1350_193-1349delinsAC MANE Select	ENSP00000394842.2:n.193-1350_193-1349delinsAC
ENST00000233612.8:c.136-1350_136-1349delinsAC	ENSP00000233612.4:n.136-1350_136-1349delinsAC
ENST00000429691.6:c.136-1350_136-1349delinsAC	ENSP00000412899.2:n.136-1350_136-1349delinsAC
ENST00000437150.6:c.193-1350_193-1349delinsAC	ENSP00000394842.2:n.193-1350_193-1349delinsAC
ENST00000446271.5:c.271-1350_271-1349delinsAC	ENSP00000393218.1:n.271-1350_271-1349delinsAC
ENST00000453113.6:c.136-1350_136-1349delinsAC	ENSP00000403805.2:n.136-1350_136-1349delinsAC
ENST00000473240.5:n.624-1350_624-1349delinsAC
ENST00000479199.1:n.260-1350_260-1349delinsAC
ENST00000481161.5:n.308-1350_308-1349delinsAC
ENST00000487445.6:n.283-1350_283-1349delinsAC
NM_012198.3:c.193-1350_193-1349delinsAC	NP_036330.1:n.193-1350_193-1349delinsAC
XM_005246446.2:c.193-1350_193-1349delinsAC	XP_005246503.1:n.193-1350_193-1349delinsAC
XM_006712398.2:c.271-1350_271-1349delinsAC	XP_006712461.1:n.271-1350_271-1349delinsAC
XM_006712399.2:c.271-1350_271-1349delinsAC	XP_006712462.1:n.271-1350_271-1349delinsAC
XM_006712400.2:c.238-1350_238-1349delinsAC	XP_006712463.1:n.238-1350_238-1349delinsAC
XM_006712401.2:c.271-1350_271-1349delinsAC	XP_006712464.1:n.271-1350_271-1349delinsAC
XM_011510926.1:c.136-1350_136-1349delinsAC	XP_011509228.1:n.136-1350_136-1349delinsAC
XM_011510927.1:c.136-1350_136-1349delinsAC	XP_011509229.1:n.136-1350_136-1349delinsAC
NM_001330265.1:c.238-1350_238-1349delinsAC	NP_001317194.1:n.238-1350_238-1349delinsAC
NM_001330266.1:c.238-1350_238-1349delinsAC	NP_001317195.1:n.238-1350_238-1349delinsAC
NM_001330267.1:c.238-1350_238-1349delinsAC	NP_001317196.1:n.238-1350_238-1349delinsAC
NM_001330268.1:c.271-1350_271-1349delinsAC	NP_001317197.1:n.271-1350_271-1349delinsAC
NM_001330270.1:c.136-1350_136-1349delinsAC	NP_001317199.1:n.136-1350_136-1349delinsAC
NM_001330271.1:c.136-1350_136-1349delinsAC	NP_001317200.1:n.136-1350_136-1349delinsAC
NM_012198.4:c.193-1350_193-1349delinsAC	NP_036330.1:n.193-1350_193-1349delinsAC
XM_005246446.3:c.193-1350_193-1349delinsAC	XP_005246503.1:n.193-1350_193-1349delinsAC
XM_006712398.4:c.271-1350_271-1349delinsAC	XP_006712461.1:n.271-1350_271-1349delinsAC
XM_006712400.4:c.238-1350_238-1349delinsAC	XP_006712463.1:n.238-1350_238-1349delinsAC
XM_011510926.2:c.136-1350_136-1349delinsAC	XP_011509228.1:n.136-1350_136-1349delinsAC
XM_017003767.1:c.136-1350_136-1349delinsAC	XP_016859256.1:n.136-1350_136-1349delinsAC
XM_017003769.2:c.271-1350_271-1349delinsAC	XP_016859258.1:n.271-1350_271-1349delinsAC
NM_012198.5:c.193-1350_193-1349delinsAC MANE Select	NP_036330.1:n.193-1350_193-1349delinsAC
NM_001330270.2:c.136-1350_136-1349delinsAC	NP_001317199.1:n.136-1350_136-1349delinsAC
NM_001330271.2:c.136-1350_136-1349delinsAC	NP_001317200.1:n.136-1350_136-1349delinsAC