Canonical Allele Identifier: CA2810026609
Gene: CA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.60150153_60150154insACAA , CM000679.2:g.60150153_60150154insACAA GRCh38
NC_000017.10:g.58227514_58227515insACAA , CM000679.1:g.58227514_58227515insACAA GRCh37
NC_000017.9:g.55582296_55582297insACAA NCBI36
NG_012050.1:g.5213_5214insACAA
NG_012050.2:g.5213_5214insACAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000300900.9:c.58+61_58+62insACAA MANE Select ENSP00000300900.3:n.58+61_58+62insACAA
ENST00000300900.8:c.58+61_58+62insACAA ENSP00000300900.3:n.58+61_58+62insACAA
ENST00000585705.5:n.151+61_151+62insACAA
ENST00000586876.1:c.58+61_58+62insACAA ENSP00000467465.1:n.58+61_58+62insACAA
ENST00000591725.1:c.-301+61_-301+62insACAA ENSP00000466964.1:n.-301+61_-301+62insACAA
NM_000717.3:c.58+61_58+62insACAA NP_000708.1:n.58+61_58+62insACAA
XM_005257639.1:c.58+61_58+62insACAA XP_005257696.1:n.58+61_58+62insACAA
NM_000717.4:c.58+61_58+62insACAA NP_000708.1:n.58+61_58+62insACAA
NR_137422.1:n.157+61_157+62insACAA
XM_005257639.3:c.58+61_58+62insACAA XP_005257696.1:n.58+61_58+62insACAA
XR_001752604.2:n.151+61_151+62insACAA
XR_001752605.2:n.151+61_151+62insACAA
XR_001752606.2:n.151+61_151+62insACAA
XR_001752607.2:n.151+61_151+62insACAA
XR_001752608.2:n.151+61_151+62insACAA
XR_001752609.2:n.151+61_151+62insACAA
XR_001752610.2:n.151+61_151+62insACAA
NM_000717.5:c.58+61_58+62insACAA MANE Select NP_000708.1:n.58+61_58+62insACAA
NR_137422.2:n.120+61_120+62insACAA