Canonical Allele Identifier: CA2810026637

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150242_60150243insACC , CM000679.2:g.60150242_60150243insACC	GRCh38
NC_000017.10:g.58227603_58227604insACC , CM000679.1:g.58227603_58227604insACC	GRCh37
NC_000017.9:g.55582385_55582386insACC	NCBI36
NG_012050.1:g.5302_5303insACC
NG_012050.2:g.5302_5303insACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.58+150_58+151insACC MANE Select	ENSP00000300900.3:n.58+150_58+151insACC
ENST00000300900.8:c.58+150_58+151insACC	ENSP00000300900.3:n.58+150_58+151insACC
ENST00000585705.5:n.151+150_151+151insACC
ENST00000586876.1:c.58+150_58+151insACC	ENSP00000467465.1:n.58+150_58+151insACC
ENST00000591725.1:c.-301+150_-301+151insACC	ENSP00000466964.1:n.-301+150_-301+151insACC
NM_000717.3:c.58+150_58+151insACC	NP_000708.1:n.58+150_58+151insACC
XM_005257639.1:c.58+150_58+151insACC	XP_005257696.1:n.58+150_58+151insACC
NM_000717.4:c.58+150_58+151insACC	NP_000708.1:n.58+150_58+151insACC
NR_137422.1:n.157+150_157+151insACC
XM_005257639.3:c.58+150_58+151insACC	XP_005257696.1:n.58+150_58+151insACC
XR_001752604.2:n.151+150_151+151insACC
XR_001752605.2:n.151+150_151+151insACC
XR_001752606.2:n.151+150_151+151insACC
XR_001752607.2:n.151+150_151+151insACC
XR_001752608.2:n.151+150_151+151insACC
XR_001752609.2:n.151+150_151+151insACC
XR_001752610.2:n.151+150_151+151insACC
NM_000717.5:c.58+150_58+151insACC MANE Select	NP_000708.1:n.58+150_58+151insACC
NR_137422.2:n.120+150_120+151insACC