Canonical Allele Identifier: CA15581187
Gene: CA1 HGNC NCBI

Linked Data

dbSNP Id: rs1532423

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.85356084A>G , CM000670.2:g.85356084A>G GRCh38
NC_000008.10:g.86268313A>G , CM000670.1:g.86268313A>G GRCh37
NC_000008.9:g.86455565A>G NCBI36
NG_016221.1:g.27030T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000517429.5:c.-24-14425T>C ENSP00000430710.1:p.=
ENST00000517590.5:c.-101-13259T>C ENSP00000429843.1:p.=
ENST00000519129.5:c.-356-4300T>C ENSP00000429688.1:p.=
ENST00000519991.5:c.-46-14425T>C ENSP00000430543.1:p.=
ENST00000520663.5:c.-123-13259T>C ENSP00000430571.1:p.=
ENST00000521846.5:c.-155-4300T>C ENSP00000430471.1:p.=
ENST00000522579.5:c.-99-6199T>C ENSP00000427852.1:p.=
ENST00000522662.5:c.-79-14276T>C ENSP00000430372.1:p.=
ENST00000522814.5:c.-105-14250T>C ENSP00000430737.1:p.=
ENST00000523022.5:c.-24-14425T>C ENSP00000429798.1:p.=
ENST00000523858.5:c.-153-4300T>C ENSP00000430975.1:p.=
ENST00000523953.5:c.-78-4300T>C ENSP00000430656.1:p.=
ENST00000524324.5:c.-24-14425T>C ENSP00000428923.1:p.=
ENST00000626824.1:c.-100-4300T>C ENSP00000486171.1:p.=
NM_001128829.3:c.-99-6199T>C NP_001122301.1:p.=
NM_001128830.3:c.-101-13259T>C NP_001122302.1:p.=
NM_001128831.3:c.-24-14425T>C NP_001122303.1:p.=
NM_001291967.1:c.-24-14425T>C NP_001278896.1:p.=
NM_001291968.1:c.-46-14425T>C NP_001278897.1:p.=
NM_001738.4:c.-78-4300T>C NP_001729.1:p.=
XM_011517584.1:c.-155-4300T>C XP_011515886.1:p.=
NM_001128829.4:c.-99-6199T>C NP_001122301.1:p.=
NM_001128830.4:c.-101-13259T>C NP_001122302.1:p.=
NM_001128831.4:c.-24-14425T>C MANE Select NP_001122303.1:p.=
NM_001291967.2:c.-24-14425T>C NP_001278896.1:p.=
NM_001291968.2:c.-46-14425T>C NP_001278897.1:p.=
NM_001738.5:c.-78-4300T>C NP_001729.1:p.=