Canonical Allele Identifier: CA626783272

Gene: CA4

Linked Data

• dbSNP Id: rs1375855951
• gnomAD v2: 17-58227466-GCT-G
• gnomAD v3: 17-60150105-GCT-G
• gnomAD v4: 17-60150105-GCT-G
• MyVariant Identifiers: chr17:g.58227467_58227468del (hg19) ; chr17:g.60150106_60150107del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150107_60150108del , CM000679.2:g.60150107_60150108del	GRCh38
NC_000017.10:g.58227468_58227469del , CM000679.1:g.58227468_58227469del	GRCh37
NC_000017.9:g.55582250_55582251del	NCBI36
NG_012050.1:g.5167_5168del
NG_012050.2:g.5167_5168del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.58+15_58+16del MANE Select	ENSP00000300900.3:n.58+15_58+16del
ENST00000300900.8:c.58+15_58+16del	ENSP00000300900.3:n.58+15_58+16del
ENST00000585705.5:n.151+15_151+16del
ENST00000586876.1:c.58+15_58+16del	ENSP00000467465.1:n.58+15_58+16del
ENST00000591725.1:c.-301+15_-301+16del	ENSP00000466964.1:n.-301+15_-301+16del
NM_000717.3:c.58+15_58+16del	NP_000708.1:n.58+15_58+16del
XM_005257639.1:c.58+15_58+16del	XP_005257696.1:n.58+15_58+16del
NM_000717.4:c.58+15_58+16del	NP_000708.1:n.58+15_58+16del
NR_137422.1:n.157+15_157+16del
XM_005257639.3:c.58+15_58+16del	XP_005257696.1:n.58+15_58+16del
XR_001752604.2:n.151+15_151+16del
XR_001752605.2:n.151+15_151+16del
XR_001752606.2:n.151+15_151+16del
XR_001752607.2:n.151+15_151+16del
XR_001752608.2:n.151+15_151+16del
XR_001752609.2:n.151+15_151+16del
XR_001752610.2:n.151+15_151+16del
NM_000717.5:c.58+15_58+16del MANE Select	NP_000708.1:n.58+15_58+16del
NR_137422.2:n.120+15_120+16del