Canonical Allele Identifier: CA2268452114

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150105_60150107delinsGCT , CM000679.2:g.60150105_60150107delinsGCT	GRCh38
NC_000017.10:g.58227466_58227468delinsGCT , CM000679.1:g.58227466_58227468delinsGCT	GRCh37
NC_000017.9:g.55582248_55582250delinsGCT	NCBI36
NG_012050.1:g.5165_5167delinsGCT
NG_012050.2:g.5165_5167delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.58+13_58+15delinsGCT MANE Select	ENSP00000300900.3:n.58+13_58+15delinsGCT
ENST00000300900.8:c.58+13_58+15delinsGCT	ENSP00000300900.3:n.58+13_58+15delinsGCT
ENST00000585705.5:n.151+13_151+15delinsGCT
ENST00000586876.1:c.58+13_58+15delinsGCT	ENSP00000467465.1:n.58+13_58+15delinsGCT
ENST00000591725.1:c.-301+13_-301+15delinsGCT	ENSP00000466964.1:n.-301+13_-301+15delinsGCT
NM_000717.3:c.58+13_58+15delinsGCT	NP_000708.1:n.58+13_58+15delinsGCT
XM_005257639.1:c.58+13_58+15delinsGCT	XP_005257696.1:n.58+13_58+15delinsGCT
NM_000717.4:c.58+13_58+15delinsGCT	NP_000708.1:n.58+13_58+15delinsGCT
NR_137422.1:n.157+13_157+15delinsGCT
XM_005257639.3:c.58+13_58+15delinsGCT	XP_005257696.1:n.58+13_58+15delinsGCT
XR_001752604.2:n.151+13_151+15delinsGCT
XR_001752605.2:n.151+13_151+15delinsGCT
XR_001752606.2:n.151+13_151+15delinsGCT
XR_001752607.2:n.151+13_151+15delinsGCT
XR_001752608.2:n.151+13_151+15delinsGCT
XR_001752609.2:n.151+13_151+15delinsGCT
XR_001752610.2:n.151+13_151+15delinsGCT
NM_000717.5:c.58+13_58+15delinsGCT MANE Select	NP_000708.1:n.58+13_58+15delinsGCT
NR_137422.2:n.120+13_120+15delinsGCT