Canonical Allele Identifier: CA2842629541
Gene: CA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.60149951C>G , CM000679.2:g.60149951C>G GRCh38
NC_000017.10:g.58227312C>G , CM000679.1:g.58227312C>G GRCh37
NC_000017.9:g.55582094C>G NCBI36
NG_012050.1:g.5011C>G
NG_012050.2:g.5011C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300900.8:c.-84C>G ENSP00000300900.3:n.-84C>G
ENST00000585705.5:n.10C>G
ENST00000586876.1:c.-84C>G ENSP00000467465.1:n.-84C>G
ENST00000591725.1:c.-442C>G ENSP00000466964.1:n.-442C>G
NM_000717.3:c.-84C>G NP_000708.1:n.-84C>G
XM_005257639.1:c.-84C>G XP_005257696.1:n.-84C>G
NM_000717.4:c.-84C>G NP_000708.1:n.-84C>G
NR_137422.1:n.16C>G
XM_005257639.3:c.-84C>G XP_005257696.1:n.-84C>G
XR_001752604.2:n.10C>G
XR_001752605.2:n.10C>G
XR_001752606.2:n.10C>G
XR_001752607.2:n.10C>G
XR_001752608.2:n.10C>G
XR_001752609.2:n.10C>G
XR_001752610.2:n.10C>G