Canonical Allele Identifier: CA2268452120

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150110_60150112delinsGGC , CM000679.2:g.60150110_60150112delinsGGC	GRCh38
NC_000017.10:g.58227471_58227473delinsGGC , CM000679.1:g.58227471_58227473delinsGGC	GRCh37
NC_000017.9:g.55582253_55582255delinsGGC	NCBI36
NG_012050.1:g.5170_5172delinsGGC
NG_012050.2:g.5170_5172delinsGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.58+18_58+20delinsGGC MANE Select	ENSP00000300900.3:n.58+18_58+20delinsGGC
ENST00000300900.8:c.58+18_58+20delinsGGC	ENSP00000300900.3:n.58+18_58+20delinsGGC
ENST00000585705.5:n.151+18_151+20delinsGGC
ENST00000586876.1:c.58+18_58+20delinsGGC	ENSP00000467465.1:n.58+18_58+20delinsGGC
ENST00000591725.1:c.-301+18_-301+20delinsGGC	ENSP00000466964.1:n.-301+18_-301+20delinsGGC
NM_000717.3:c.58+18_58+20delinsGGC	NP_000708.1:n.58+18_58+20delinsGGC
XM_005257639.1:c.58+18_58+20delinsGGC	XP_005257696.1:n.58+18_58+20delinsGGC
NM_000717.4:c.58+18_58+20delinsGGC	NP_000708.1:n.58+18_58+20delinsGGC
NR_137422.1:n.157+18_157+20delinsGGC
XM_005257639.3:c.58+18_58+20delinsGGC	XP_005257696.1:n.58+18_58+20delinsGGC
XR_001752604.2:n.151+18_151+20delinsGGC
XR_001752605.2:n.151+18_151+20delinsGGC
XR_001752606.2:n.151+18_151+20delinsGGC
XR_001752607.2:n.151+18_151+20delinsGGC
XR_001752608.2:n.151+18_151+20delinsGGC
XR_001752609.2:n.151+18_151+20delinsGGC
XR_001752610.2:n.151+18_151+20delinsGGC
NM_000717.5:c.58+18_58+20delinsGGC MANE Select	NP_000708.1:n.58+18_58+20delinsGGC
NR_137422.2:n.120+18_120+20delinsGGC