Canonical Allele Identifier: CA371418403
Gene: CA1 HGNC NCBI

Linked Data

gnomAD v4: 8-85328568-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.85328568A>T , CM000670.2:g.85328568A>T GRCh38
NC_000008.10:g.86240797A>T , CM000670.1:g.86240797A>T GRCh37
NC_000008.9:g.86428049A>T NCBI36
NG_016221.1:g.54546T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000523022.6:c.778T>A MANE Select ENSP00000429798.1:p.Ser260Thr
ENST00000431316.3:c.778T>A ENSP00000392338.1:p.Ser260Thr
ENST00000521679.5:c.527T>A
ENST00000522389.5:c.376T>A ENSP00000427773.1:p.Ser126Thr
ENST00000523022.5:c.778T>A ENSP00000429798.1:p.Ser260Thr
ENST00000523953.5:c.778T>A ENSP00000430656.1:p.Ser260Thr
ENST00000524324.5:c.580T>A ENSP00000428923.1:p.Ser194Thr
ENST00000542576.5:c.778T>A ENSP00000443517.1:p.Ser260Thr
ENST00000626824.1:c.376T>A ENSP00000486171.1:p.Ser126Thr
NM_001128829.3:c.778T>A NP_001122301.1:p.Ser260Thr
NM_001128830.3:c.778T>A NP_001122302.1:p.Ser260Thr
NM_001128831.3:c.778T>A NP_001122303.1:p.Ser260Thr
NM_001164830.1:c.778T>A NP_001158302.1:p.Ser260Thr
NM_001291967.1:c.580T>A NP_001278896.1:p.Ser194Thr
NM_001291968.1:c.439T>A NP_001278897.1:p.Ser147Thr
NM_001738.4:c.778T>A NP_001729.1:p.Ser260Thr
XM_011517584.1:c.778T>A XP_011515886.1:p.Ser260Thr
NM_001128829.4:c.778T>A NP_001122301.1:p.Ser260Thr
NM_001128830.4:c.778T>A NP_001122302.1:p.Ser260Thr
NM_001128831.4:c.778T>A MANE Select NP_001122303.1:p.Ser260Thr
NM_001164830.2:c.778T>A NP_001158302.1:p.Ser260Thr
NM_001291967.2:c.580T>A NP_001278896.1:p.Ser194Thr
NM_001291968.2:c.439T>A NP_001278897.1:p.Ser147Thr
NM_001738.5:c.778T>A NP_001729.1:p.Ser260Thr