Canonical Allele Identifier: CA2810026587

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150118_60150119insACT , CM000679.2:g.60150118_60150119insACT	GRCh38
NC_000017.10:g.58227479_58227480insACT , CM000679.1:g.58227479_58227480insACT	GRCh37
NC_000017.9:g.55582261_55582262insACT	NCBI36
NG_012050.1:g.5178_5179insACT
NG_012050.2:g.5178_5179insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.58+26_58+27insACT MANE Select	ENSP00000300900.3:n.58+26_58+27insACT
ENST00000300900.8:c.58+26_58+27insACT	ENSP00000300900.3:n.58+26_58+27insACT
ENST00000585705.5:n.151+26_151+27insACT
ENST00000586876.1:c.58+26_58+27insACT	ENSP00000467465.1:n.58+26_58+27insACT
ENST00000591725.1:c.-301+26_-301+27insACT	ENSP00000466964.1:n.-301+26_-301+27insACT
NM_000717.3:c.58+26_58+27insACT	NP_000708.1:n.58+26_58+27insACT
XM_005257639.1:c.58+26_58+27insACT	XP_005257696.1:n.58+26_58+27insACT
NM_000717.4:c.58+26_58+27insACT	NP_000708.1:n.58+26_58+27insACT
NR_137422.1:n.157+26_157+27insACT
XM_005257639.3:c.58+26_58+27insACT	XP_005257696.1:n.58+26_58+27insACT
XR_001752604.2:n.151+26_151+27insACT
XR_001752605.2:n.151+26_151+27insACT
XR_001752606.2:n.151+26_151+27insACT
XR_001752607.2:n.151+26_151+27insACT
XR_001752608.2:n.151+26_151+27insACT
XR_001752609.2:n.151+26_151+27insACT
XR_001752610.2:n.151+26_151+27insACT
NM_000717.5:c.58+26_58+27insACT MANE Select	NP_000708.1:n.58+26_58+27insACT
NR_137422.2:n.120+26_120+27insACT