Canonical Allele Identifier: CA1799299514
Gene: CA1 HGNC NCBI

Linked Data

dbSNP Id: rs1809597306

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.85356098A>G , CM000670.2:g.85356098A>G GRCh38
NC_000008.10:g.86268327A>G , CM000670.1:g.86268327A>G GRCh37
NC_000008.9:g.86455579A>G NCBI36
NG_016221.1:g.27016T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000523022.6:c.-24-14439T>C MANE Select ENSP00000429798.1:n.-24-14439T>C
ENST00000517429.5:c.-24-14439T>C ENSP00000430710.1:n.-24-14439T>C
ENST00000517590.5:c.-101-13273T>C ENSP00000429843.1:n.-101-13273T>C
ENST00000518341.5:n.69-14439T>C
ENST00000519129.5:c.-356-4314T>C ENSP00000429688.1:n.-356-4314T>C
ENST00000519991.5:c.-46-14439T>C ENSP00000430543.1:n.-46-14439T>C
ENST00000520093.5:n.69-14439T>C
ENST00000520663.5:c.-123-13273T>C ENSP00000430571.1:n.-123-13273T>C
ENST00000520990.5:n.69-13273T>C
ENST00000521846.5:c.-155-4314T>C ENSP00000430471.1:n.-155-4314T>C
ENST00000522579.5:c.-99-6213T>C ENSP00000427852.1:n.-99-6213T>C
ENST00000522662.5:c.-79-14290T>C ENSP00000430372.1:n.-79-14290T>C
ENST00000522814.5:c.-105-14264T>C ENSP00000430737.1:n.-105-14264T>C
ENST00000523022.5:c.-24-14439T>C ENSP00000429798.1:n.-24-14439T>C
ENST00000523858.5:c.-153-4314T>C ENSP00000430975.1:n.-153-4314T>C
ENST00000523953.5:c.-78-4314T>C ENSP00000430656.1:n.-78-4314T>C
ENST00000524324.5:c.-24-14439T>C ENSP00000428923.1:n.-24-14439T>C
ENST00000626824.1:c.-100-4314T>C ENSP00000486171.1:n.-100-4314T>C
NM_001128829.3:c.-99-6213T>C NP_001122301.1:n.-99-6213T>C
NM_001128830.3:c.-101-13273T>C NP_001122302.1:n.-101-13273T>C
NM_001128831.3:c.-24-14439T>C NP_001122303.1:n.-24-14439T>C
NM_001291967.1:c.-24-14439T>C NP_001278896.1:n.-24-14439T>C
NM_001291968.1:c.-46-14439T>C NP_001278897.1:n.-46-14439T>C
NM_001738.4:c.-78-4314T>C NP_001729.1:n.-78-4314T>C
XM_011517584.1:c.-155-4314T>C XP_011515886.1:n.-155-4314T>C
NM_001128829.4:c.-99-6213T>C NP_001122301.1:n.-99-6213T>C
NM_001128830.4:c.-101-13273T>C NP_001122302.1:n.-101-13273T>C
NM_001128831.4:c.-24-14439T>C MANE Select NP_001122303.1:n.-24-14439T>C
NM_001291967.2:c.-24-14439T>C NP_001278896.1:n.-24-14439T>C
NM_001291968.2:c.-46-14439T>C NP_001278897.1:n.-46-14439T>C
NM_001738.5:c.-78-4314T>C NP_001729.1:n.-78-4314T>C