Canonical Allele Identifier: CA1799299590

Gene: CA1

Linked Data

• dbSNP Id: rs1809600691

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.85356182_85356191del , CM000670.2:g.85356182_85356191del	GRCh38
NC_000008.10:g.86268411_86268420del , CM000670.1:g.86268411_86268420del	GRCh37
NC_000008.9:g.86455663_86455672del	NCBI36
NG_016221.1:g.26923_26932del

Transcript Alleles

HGVS	Amino-acid change
ENST00000523022.6:c.-24-14532_-24-14523del MANE Select	ENSP00000429798.1:n.-24-14532_-24-14523del
ENST00000517429.5:c.-24-14532_-24-14523del	ENSP00000430710.1:n.-24-14532_-24-14523del
ENST00000517590.5:c.-101-13366_-101-13357del	ENSP00000429843.1:n.-101-13366_-101-13357del
ENST00000518341.5:n.69-14532_69-14523del
ENST00000519129.5:c.-356-4407_-356-4398del	ENSP00000429688.1:n.-356-4407_-356-4398del
ENST00000519991.5:c.-46-14532_-46-14523del	ENSP00000430543.1:n.-46-14532_-46-14523del
ENST00000520093.5:n.69-14532_69-14523del
ENST00000520663.5:c.-123-13366_-123-13357del	ENSP00000430571.1:n.-123-13366_-123-13357del
ENST00000520990.5:n.69-13366_69-13357del
ENST00000521846.5:c.-155-4407_-155-4398del	ENSP00000430471.1:n.-155-4407_-155-4398del
ENST00000522579.5:c.-99-6306_-99-6297del	ENSP00000427852.1:n.-99-6306_-99-6297del
ENST00000522662.5:c.-79-14383_-79-14374del	ENSP00000430372.1:n.-79-14383_-79-14374del
ENST00000522814.5:c.-105-14357_-105-14348del	ENSP00000430737.1:n.-105-14357_-105-14348del
ENST00000523022.5:c.-24-14532_-24-14523del	ENSP00000429798.1:n.-24-14532_-24-14523del
ENST00000523858.5:c.-153-4407_-153-4398del	ENSP00000430975.1:n.-153-4407_-153-4398del
ENST00000523953.5:c.-78-4407_-78-4398del	ENSP00000430656.1:n.-78-4407_-78-4398del
ENST00000524324.5:c.-24-14532_-24-14523del	ENSP00000428923.1:n.-24-14532_-24-14523del
ENST00000626824.1:c.-100-4407_-100-4398del	ENSP00000486171.1:n.-100-4407_-100-4398del
NM_001128829.3:c.-99-6306_-99-6297del	NP_001122301.1:n.-99-6306_-99-6297del
NM_001128830.3:c.-101-13366_-101-13357del	NP_001122302.1:n.-101-13366_-101-13357del
NM_001128831.3:c.-24-14532_-24-14523del	NP_001122303.1:n.-24-14532_-24-14523del
NM_001291967.1:c.-24-14532_-24-14523del	NP_001278896.1:n.-24-14532_-24-14523del
NM_001291968.1:c.-46-14532_-46-14523del	NP_001278897.1:n.-46-14532_-46-14523del
NM_001738.4:c.-78-4407_-78-4398del	NP_001729.1:n.-78-4407_-78-4398del
XM_011517584.1:c.-155-4407_-155-4398del	XP_011515886.1:n.-155-4407_-155-4398del
NM_001128829.4:c.-99-6306_-99-6297del	NP_001122301.1:n.-99-6306_-99-6297del
NM_001128830.4:c.-101-13366_-101-13357del	NP_001122302.1:n.-101-13366_-101-13357del
NM_001128831.4:c.-24-14532_-24-14523del MANE Select	NP_001122303.1:n.-24-14532_-24-14523del
NM_001291967.2:c.-24-14532_-24-14523del	NP_001278896.1:n.-24-14532_-24-14523del
NM_001291968.2:c.-46-14532_-46-14523del	NP_001278897.1:n.-46-14532_-46-14523del
NM_001738.5:c.-78-4407_-78-4398del	NP_001729.1:n.-78-4407_-78-4398del