Canonical Allele Identifier: CA914193208

Gene: CA4

Linked Data

• dbSNP Id: rs1567725887
• gnomAD v2: 17-58227713-GCGAGA-G
• gnomAD v3: 17-60150352-GCGAGA-G
• gnomAD v4: 17-60150352-GCGAGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150357_60150361del , CM000679.2:g.60150357_60150361del	GRCh38
NC_000017.10:g.58227718_58227722del , CM000679.1:g.58227718_58227722del	GRCh37
NC_000017.9:g.55582500_55582504del	NCBI36
NG_012050.1:g.5417_5421del
NG_012050.2:g.5417_5421del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.58+265_58+269del MANE Select	ENSP00000300900.3:n.58+265_58+269del
ENST00000300900.8:c.58+265_58+269del	ENSP00000300900.3:n.58+265_58+269del
ENST00000585705.5:n.151+265_151+269del
ENST00000586876.1:c.58+265_58+269del	ENSP00000467465.1:n.58+265_58+269del
ENST00000591725.1:c.-301+265_-301+269del	ENSP00000466964.1:n.-301+265_-301+269del
NM_000717.3:c.58+265_58+269del	NP_000708.1:n.58+265_58+269del
XM_005257639.1:c.58+265_58+269del	XP_005257696.1:n.58+265_58+269del
NM_000717.4:c.58+265_58+269del	NP_000708.1:n.58+265_58+269del
NR_137422.1:n.157+265_157+269del
XM_005257639.3:c.58+265_58+269del	XP_005257696.1:n.58+265_58+269del
XR_001752604.2:n.151+265_151+269del
XR_001752605.2:n.151+265_151+269del
XR_001752606.2:n.151+265_151+269del
XR_001752607.2:n.151+265_151+269del
XR_001752608.2:n.151+265_151+269del
XR_001752609.2:n.151+265_151+269del
XR_001752610.2:n.151+265_151+269del
NM_000717.5:c.58+265_58+269del MANE Select	NP_000708.1:n.58+265_58+269del
NR_137422.2:n.120+265_120+269del