Canonical Allele Identifier: CA2268452162

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150169_60150170delinsTC , CM000679.2:g.60150169_60150170delinsTC	GRCh38
NC_000017.10:g.58227530_58227531delinsTC , CM000679.1:g.58227530_58227531delinsTC	GRCh37
NC_000017.9:g.55582312_55582313delinsTC	NCBI36
NG_012050.1:g.5229_5230delinsTC
NG_012050.2:g.5229_5230delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.58+77_58+78delinsTC MANE Select	ENSP00000300900.3:n.58+77_58+78delinsTC
ENST00000300900.8:c.58+77_58+78delinsTC	ENSP00000300900.3:n.58+77_58+78delinsTC
ENST00000585705.5:n.151+77_151+78delinsTC
ENST00000586876.1:c.58+77_58+78delinsTC	ENSP00000467465.1:n.58+77_58+78delinsTC
ENST00000591725.1:c.-301+77_-301+78delinsTC	ENSP00000466964.1:n.-301+77_-301+78delinsTC
NM_000717.3:c.58+77_58+78delinsTC	NP_000708.1:n.58+77_58+78delinsTC
XM_005257639.1:c.58+77_58+78delinsTC	XP_005257696.1:n.58+77_58+78delinsTC
NM_000717.4:c.58+77_58+78delinsTC	NP_000708.1:n.58+77_58+78delinsTC
NR_137422.1:n.157+77_157+78delinsTC
XM_005257639.3:c.58+77_58+78delinsTC	XP_005257696.1:n.58+77_58+78delinsTC
XR_001752604.2:n.151+77_151+78delinsTC
XR_001752605.2:n.151+77_151+78delinsTC
XR_001752606.2:n.151+77_151+78delinsTC
XR_001752607.2:n.151+77_151+78delinsTC
XR_001752608.2:n.151+77_151+78delinsTC
XR_001752609.2:n.151+77_151+78delinsTC
XR_001752610.2:n.151+77_151+78delinsTC
NM_000717.5:c.58+77_58+78delinsTC MANE Select	NP_000708.1:n.58+77_58+78delinsTC
NR_137422.2:n.120+77_120+78delinsTC