Canonical Allele Identifier: CA2810026623

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150173_60150174insA , CM000679.2:g.60150173_60150174insA	GRCh38
NC_000017.10:g.58227534_58227535insA , CM000679.1:g.58227534_58227535insA	GRCh37
NC_000017.9:g.55582316_55582317insA	NCBI36
NG_012050.1:g.5233_5234insA
NG_012050.2:g.5233_5234insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.58+81_58+82insA MANE Select	ENSP00000300900.3:n.58+81_58+82insA
ENST00000300900.8:c.58+81_58+82insA	ENSP00000300900.3:n.58+81_58+82insA
ENST00000585705.5:n.151+81_151+82insA
ENST00000586876.1:c.58+81_58+82insA	ENSP00000467465.1:n.58+81_58+82insA
ENST00000591725.1:c.-301+81_-301+82insA	ENSP00000466964.1:n.-301+81_-301+82insA
NM_000717.3:c.58+81_58+82insA	NP_000708.1:n.58+81_58+82insA
XM_005257639.1:c.58+81_58+82insA	XP_005257696.1:n.58+81_58+82insA
NM_000717.4:c.58+81_58+82insA	NP_000708.1:n.58+81_58+82insA
NR_137422.1:n.157+81_157+82insA
XM_005257639.3:c.58+81_58+82insA	XP_005257696.1:n.58+81_58+82insA
XR_001752604.2:n.151+81_151+82insA
XR_001752605.2:n.151+81_151+82insA
XR_001752606.2:n.151+81_151+82insA
XR_001752607.2:n.151+81_151+82insA
XR_001752608.2:n.151+81_151+82insA
XR_001752609.2:n.151+81_151+82insA
XR_001752610.2:n.151+81_151+82insA
NM_000717.5:c.58+81_58+82insA MANE Select	NP_000708.1:n.58+81_58+82insA
NR_137422.2:n.120+81_120+82insA