Canonical Allele Identifier: CA2639096441
Gene: CA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.60150244_60150245insGAA , CM000679.2:g.60150244_60150245insGAA GRCh38
NC_000017.10:g.58227605_58227606insGAA , CM000679.1:g.58227605_58227606insGAA GRCh37
NC_000017.9:g.55582387_55582388insGAA NCBI36
NG_012050.1:g.5304_5305insGAA
NG_012050.2:g.5304_5305insGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000300900.9:c.58+152_58+153insGAA MANE Select ENSP00000300900.3:n.58+152_58+153insGAA
ENST00000300900.8:c.58+152_58+153insGAA ENSP00000300900.3:n.58+152_58+153insGAA
ENST00000585705.5:n.151+152_151+153insGAA
ENST00000586876.1:c.58+152_58+153insGAA ENSP00000467465.1:n.58+152_58+153insGAA
ENST00000591725.1:c.-301+152_-301+153insGAA ENSP00000466964.1:n.-301+152_-301+153insGAA
NM_000717.3:c.58+152_58+153insGAA NP_000708.1:n.58+152_58+153insGAA
XM_005257639.1:c.58+152_58+153insGAA XP_005257696.1:n.58+152_58+153insGAA
NM_000717.4:c.58+152_58+153insGAA NP_000708.1:n.58+152_58+153insGAA
NR_137422.1:n.157+152_157+153insGAA
XM_005257639.3:c.58+152_58+153insGAA XP_005257696.1:n.58+152_58+153insGAA
XR_001752604.2:n.151+152_151+153insGAA
XR_001752605.2:n.151+152_151+153insGAA
XR_001752606.2:n.151+152_151+153insGAA
XR_001752607.2:n.151+152_151+153insGAA
XR_001752608.2:n.151+152_151+153insGAA
XR_001752609.2:n.151+152_151+153insGAA
XR_001752610.2:n.151+152_151+153insGAA
NM_000717.5:c.58+152_58+153insGAA MANE Select NP_000708.1:n.58+152_58+153insGAA
NR_137422.2:n.120+152_120+153insGAA