Canonical Allele Identifier: CA2810026607

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150150_60150151insACAT , CM000679.2:g.60150150_60150151insACAT	GRCh38
NC_000017.10:g.58227511_58227512insACAT , CM000679.1:g.58227511_58227512insACAT	GRCh37
NC_000017.9:g.55582293_55582294insACAT	NCBI36
NG_012050.1:g.5210_5211insACAT
NG_012050.2:g.5210_5211insACAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.58+58_58+59insACAT MANE Select	ENSP00000300900.3:n.58+58_58+59insACAT
ENST00000300900.8:c.58+58_58+59insACAT	ENSP00000300900.3:n.58+58_58+59insACAT
ENST00000585705.5:n.151+58_151+59insACAT
ENST00000586876.1:c.58+58_58+59insACAT	ENSP00000467465.1:n.58+58_58+59insACAT
ENST00000591725.1:c.-301+58_-301+59insACAT	ENSP00000466964.1:n.-301+58_-301+59insACAT
NM_000717.3:c.58+58_58+59insACAT	NP_000708.1:n.58+58_58+59insACAT
XM_005257639.1:c.58+58_58+59insACAT	XP_005257696.1:n.58+58_58+59insACAT
NM_000717.4:c.58+58_58+59insACAT	NP_000708.1:n.58+58_58+59insACAT
NR_137422.1:n.157+58_157+59insACAT
XM_005257639.3:c.58+58_58+59insACAT	XP_005257696.1:n.58+58_58+59insACAT
XR_001752604.2:n.151+58_151+59insACAT
XR_001752605.2:n.151+58_151+59insACAT
XR_001752606.2:n.151+58_151+59insACAT
XR_001752607.2:n.151+58_151+59insACAT
XR_001752608.2:n.151+58_151+59insACAT
XR_001752609.2:n.151+58_151+59insACAT
XR_001752610.2:n.151+58_151+59insACAT
NM_000717.5:c.58+58_58+59insACAT MANE Select	NP_000708.1:n.58+58_58+59insACAT
NR_137422.2:n.120+58_120+59insACAT