Canonical Allele Identifier: CA2810026622

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150171_60150172insAA , CM000679.2:g.60150171_60150172insAA	GRCh38
NC_000017.10:g.58227532_58227533insAA , CM000679.1:g.58227532_58227533insAA	GRCh37
NC_000017.9:g.55582314_55582315insAA	NCBI36
NG_012050.1:g.5231_5232insAA
NG_012050.2:g.5231_5232insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.58+79_58+80insAA MANE Select	ENSP00000300900.3:n.58+79_58+80insAA
ENST00000300900.8:c.58+79_58+80insAA	ENSP00000300900.3:n.58+79_58+80insAA
ENST00000585705.5:n.151+79_151+80insAA
ENST00000586876.1:c.58+79_58+80insAA	ENSP00000467465.1:n.58+79_58+80insAA
ENST00000591725.1:c.-301+79_-301+80insAA	ENSP00000466964.1:n.-301+79_-301+80insAA
NM_000717.3:c.58+79_58+80insAA	NP_000708.1:n.58+79_58+80insAA
XM_005257639.1:c.58+79_58+80insAA	XP_005257696.1:n.58+79_58+80insAA
NM_000717.4:c.58+79_58+80insAA	NP_000708.1:n.58+79_58+80insAA
NR_137422.1:n.157+79_157+80insAA
XM_005257639.3:c.58+79_58+80insAA	XP_005257696.1:n.58+79_58+80insAA
XR_001752604.2:n.151+79_151+80insAA
XR_001752605.2:n.151+79_151+80insAA
XR_001752606.2:n.151+79_151+80insAA
XR_001752607.2:n.151+79_151+80insAA
XR_001752608.2:n.151+79_151+80insAA
XR_001752609.2:n.151+79_151+80insAA
XR_001752610.2:n.151+79_151+80insAA
NM_000717.5:c.58+79_58+80insAA MANE Select	NP_000708.1:n.58+79_58+80insAA
NR_137422.2:n.120+79_120+80insAA