Canonical Allele Identifier: CA2810026589

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150123_60150124insACA , CM000679.2:g.60150123_60150124insACA	GRCh38
NC_000017.10:g.58227484_58227485insACA , CM000679.1:g.58227484_58227485insACA	GRCh37
NC_000017.9:g.55582266_55582267insACA	NCBI36
NG_012050.1:g.5183_5184insACA
NG_012050.2:g.5183_5184insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.58+31_58+32insACA MANE Select	ENSP00000300900.3:n.58+31_58+32insACA
ENST00000300900.8:c.58+31_58+32insACA	ENSP00000300900.3:n.58+31_58+32insACA
ENST00000585705.5:n.151+31_151+32insACA
ENST00000586876.1:c.58+31_58+32insACA	ENSP00000467465.1:n.58+31_58+32insACA
ENST00000591725.1:c.-301+31_-301+32insACA	ENSP00000466964.1:n.-301+31_-301+32insACA
NM_000717.3:c.58+31_58+32insACA	NP_000708.1:n.58+31_58+32insACA
XM_005257639.1:c.58+31_58+32insACA	XP_005257696.1:n.58+31_58+32insACA
NM_000717.4:c.58+31_58+32insACA	NP_000708.1:n.58+31_58+32insACA
NR_137422.1:n.157+31_157+32insACA
XM_005257639.3:c.58+31_58+32insACA	XP_005257696.1:n.58+31_58+32insACA
XR_001752604.2:n.151+31_151+32insACA
XR_001752605.2:n.151+31_151+32insACA
XR_001752606.2:n.151+31_151+32insACA
XR_001752607.2:n.151+31_151+32insACA
XR_001752608.2:n.151+31_151+32insACA
XR_001752609.2:n.151+31_151+32insACA
XR_001752610.2:n.151+31_151+32insACA
NM_000717.5:c.58+31_58+32insACA MANE Select	NP_000708.1:n.58+31_58+32insACA
NR_137422.2:n.120+31_120+32insACA