Canonical Allele Identifier: CA2810026658

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150291_60150294del , CM000679.2:g.60150291_60150294del	GRCh38
NC_000017.10:g.58227652_58227655del , CM000679.1:g.58227652_58227655del	GRCh37
NC_000017.9:g.55582434_55582437del	NCBI36
NG_012050.1:g.5351_5354del
NG_012050.2:g.5351_5354del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.58+199_58+202del MANE Select	ENSP00000300900.3:n.58+199_58+202del
ENST00000300900.8:c.58+199_58+202del	ENSP00000300900.3:n.58+199_58+202del
ENST00000585705.5:n.151+199_151+202del
ENST00000586876.1:c.58+199_58+202del	ENSP00000467465.1:n.58+199_58+202del
ENST00000591725.1:c.-301+199_-301+202del	ENSP00000466964.1:n.-301+199_-301+202del
NM_000717.3:c.58+199_58+202del	NP_000708.1:n.58+199_58+202del
XM_005257639.1:c.58+199_58+202del	XP_005257696.1:n.58+199_58+202del
NM_000717.4:c.58+199_58+202del	NP_000708.1:n.58+199_58+202del
NR_137422.1:n.157+199_157+202del
XM_005257639.3:c.58+199_58+202del	XP_005257696.1:n.58+199_58+202del
XR_001752604.2:n.151+199_151+202del
XR_001752605.2:n.151+199_151+202del
XR_001752606.2:n.151+199_151+202del
XR_001752607.2:n.151+199_151+202del
XR_001752608.2:n.151+199_151+202del
XR_001752609.2:n.151+199_151+202del
XR_001752610.2:n.151+199_151+202del
NM_000717.5:c.58+199_58+202del MANE Select	NP_000708.1:n.58+199_58+202del
NR_137422.2:n.120+199_120+202del