Canonical Allele Identifier: CA4795969
Gene: CA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.85333547G>A , CM000670.2:g.85333547G>A GRCh38
NC_000008.10:g.86245776G>A , CM000670.1:g.86245776G>A GRCh37
NC_000008.9:g.86433028G>A NCBI36
NG_016221.1:g.49567C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001128831.4:c.428C>T MANE Select NP_001122303.1:p.Ala143Val
ENST00000523022.6:c.428C>T MANE Select ENSP00000429798.1:p.Ala143Val
NM_001128829.3:c.428C>T NP_001122301.1:p.Ala143Val
NM_001128829.4:c.428C>T NP_001122301.1:p.Ala143Val
NM_001128830.3:c.428C>T NP_001122302.1:p.Ala143Val
NM_001128830.4:c.428C>T NP_001122302.1:p.Ala143Val
NM_001128831.3:c.428C>T NP_001122303.1:p.Ala143Val
NM_001164830.1:c.428C>T NP_001158302.1:p.Ala143Val
NM_001164830.2:c.428C>T NP_001158302.1:p.Ala143Val
NM_001291967.1:c.230C>T NP_001278896.1:p.Ala77Val
NM_001291967.2:c.230C>T NP_001278896.1:p.Ala77Val
NM_001291968.1:c.89C>T NP_001278897.1:p.Ala30Val
NM_001291968.2:c.89C>T NP_001278897.1:p.Ala30Val
NM_001738.4:c.428C>T NP_001729.1:p.Ala143Val
NM_001738.5:c.428C>T NP_001729.1:p.Ala143Val
ENST00000431316.3:c.428C>T ENSP00000392338.1:p.Ala143Val
ENST00000517429.5:c.*233C>T ENSP00000430710.1:n.*233C>T
ENST00000517590.5:c.428C>T ENSP00000429843.1:p.Ala143Val
ENST00000517618.5:c.428C>T ENSP00000430861.1:p.Ala143Val
ENST00000518233.5:n.151C>T
ENST00000518341.5:n.636C>T
ENST00000519991.5:c.89C>T ENSP00000430543.1:p.Ala30Val
ENST00000520663.5:c.89C>T ENSP00000430571.1:p.Ala30Val
ENST00000521679.5:c.237C>T
ENST00000521846.5:c.428C>T ENSP00000430471.1:p.Ala143Val
ENST00000522389.5:c.89C>T ENSP00000427773.1:p.Ala30Val
ENST00000522579.5:c.428C>T ENSP00000427852.1:p.Ala143Val
ENST00000522814.5:c.428C>T ENSP00000430737.1:p.Ala143Val
ENST00000523022.5:c.428C>T ENSP00000429798.1:p.Ala143Val
ENST00000523712.5:n.342C>T
ENST00000523953.5:c.428C>T ENSP00000430656.1:p.Ala143Val
ENST00000524324.5:c.230C>T ENSP00000428923.1:p.Ala77Val
ENST00000542576.5:c.428C>T ENSP00000443517.1:p.Ala143Val
ENST00000626824.1:c.89C>T ENSP00000486171.1:p.Ala30Val
XM_011517584.1:c.428C>T XP_011515886.1:p.Ala143Val