Canonical Allele Identifier: CA2810026656

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150286_60150287insA , CM000679.2:g.60150286_60150287insA	GRCh38
NC_000017.10:g.58227647_58227648insA , CM000679.1:g.58227647_58227648insA	GRCh37
NC_000017.9:g.55582429_55582430insA	NCBI36
NG_012050.1:g.5346_5347insA
NG_012050.2:g.5346_5347insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.58+194_58+195insA MANE Select	ENSP00000300900.3:n.58+194_58+195insA
ENST00000300900.8:c.58+194_58+195insA	ENSP00000300900.3:n.58+194_58+195insA
ENST00000585705.5:n.151+194_151+195insA
ENST00000586876.1:c.58+194_58+195insA	ENSP00000467465.1:n.58+194_58+195insA
ENST00000591725.1:c.-301+194_-301+195insA	ENSP00000466964.1:n.-301+194_-301+195insA
NM_000717.3:c.58+194_58+195insA	NP_000708.1:n.58+194_58+195insA
XM_005257639.1:c.58+194_58+195insA	XP_005257696.1:n.58+194_58+195insA
NM_000717.4:c.58+194_58+195insA	NP_000708.1:n.58+194_58+195insA
NR_137422.1:n.157+194_157+195insA
XM_005257639.3:c.58+194_58+195insA	XP_005257696.1:n.58+194_58+195insA
XR_001752604.2:n.151+194_151+195insA
XR_001752605.2:n.151+194_151+195insA
XR_001752606.2:n.151+194_151+195insA
XR_001752607.2:n.151+194_151+195insA
XR_001752608.2:n.151+194_151+195insA
XR_001752609.2:n.151+194_151+195insA
XR_001752610.2:n.151+194_151+195insA
NM_000717.5:c.58+194_58+195insA MANE Select	NP_000708.1:n.58+194_58+195insA
NR_137422.2:n.120+194_120+195insA