Canonical Allele Identifier: CA1799299643

Gene: CA1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.85356276_85356277delinsGT , CM000670.2:g.85356276_85356277delinsGT	GRCh38
NC_000008.10:g.86268505_86268506delinsGT , CM000670.1:g.86268505_86268506delinsGT	GRCh37
NC_000008.9:g.86455757_86455758delinsGT	NCBI36
NG_016221.1:g.26837_26838delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523022.6:c.-24-14618_-24-14617delinsAC MANE Select	ENSP00000429798.1:n.-24-14618_-24-14617delinsAC
ENST00000517429.5:c.-24-14618_-24-14617delinsAC	ENSP00000430710.1:n.-24-14618_-24-14617delinsAC
ENST00000517590.5:c.-101-13452_-101-13451delinsAC	ENSP00000429843.1:n.-101-13452_-101-13451delinsAC
ENST00000518341.5:n.69-14618_69-14617delinsAC
ENST00000519129.5:c.-356-4493_-356-4492delinsAC	ENSP00000429688.1:n.-356-4493_-356-4492delinsAC
ENST00000519991.5:c.-46-14618_-46-14617delinsAC	ENSP00000430543.1:n.-46-14618_-46-14617delinsAC
ENST00000520093.5:n.69-14618_69-14617delinsAC
ENST00000520663.5:c.-123-13452_-123-13451delinsAC	ENSP00000430571.1:n.-123-13452_-123-13451delinsAC
ENST00000520990.5:n.69-13452_69-13451delinsAC
ENST00000521846.5:c.-155-4493_-155-4492delinsAC	ENSP00000430471.1:n.-155-4493_-155-4492delinsAC
ENST00000522579.5:c.-99-6392_-99-6391delinsAC	ENSP00000427852.1:n.-99-6392_-99-6391delinsAC
ENST00000522662.5:c.-79-14469_-79-14468delinsAC	ENSP00000430372.1:n.-79-14469_-79-14468delinsAC
ENST00000522814.5:c.-105-14443_-105-14442delinsAC	ENSP00000430737.1:n.-105-14443_-105-14442delinsAC
ENST00000523022.5:c.-24-14618_-24-14617delinsAC	ENSP00000429798.1:n.-24-14618_-24-14617delinsAC
ENST00000523858.5:c.-153-4493_-153-4492delinsAC	ENSP00000430975.1:n.-153-4493_-153-4492delinsAC
ENST00000523953.5:c.-78-4493_-78-4492delinsAC	ENSP00000430656.1:n.-78-4493_-78-4492delinsAC
ENST00000524324.5:c.-24-14618_-24-14617delinsAC	ENSP00000428923.1:n.-24-14618_-24-14617delinsAC
ENST00000626824.1:c.-100-4493_-100-4492delinsAC	ENSP00000486171.1:n.-100-4493_-100-4492delinsAC
NM_001128829.3:c.-99-6392_-99-6391delinsAC	NP_001122301.1:n.-99-6392_-99-6391delinsAC
NM_001128830.3:c.-101-13452_-101-13451delinsAC	NP_001122302.1:n.-101-13452_-101-13451delinsAC
NM_001128831.3:c.-24-14618_-24-14617delinsAC	NP_001122303.1:n.-24-14618_-24-14617delinsAC
NM_001291967.1:c.-24-14618_-24-14617delinsAC	NP_001278896.1:n.-24-14618_-24-14617delinsAC
NM_001291968.1:c.-46-14618_-46-14617delinsAC	NP_001278897.1:n.-46-14618_-46-14617delinsAC
NM_001738.4:c.-78-4493_-78-4492delinsAC	NP_001729.1:n.-78-4493_-78-4492delinsAC
XM_011517584.1:c.-155-4493_-155-4492delinsAC	XP_011515886.1:n.-155-4493_-155-4492delinsAC
NM_001128829.4:c.-99-6392_-99-6391delinsAC	NP_001122301.1:n.-99-6392_-99-6391delinsAC
NM_001128830.4:c.-101-13452_-101-13451delinsAC	NP_001122302.1:n.-101-13452_-101-13451delinsAC
NM_001128831.4:c.-24-14618_-24-14617delinsAC MANE Select	NP_001122303.1:n.-24-14618_-24-14617delinsAC
NM_001291967.2:c.-24-14618_-24-14617delinsAC	NP_001278896.1:n.-24-14618_-24-14617delinsAC
NM_001291968.2:c.-46-14618_-46-14617delinsAC	NP_001278897.1:n.-46-14618_-46-14617delinsAC
NM_001738.5:c.-78-4493_-78-4492delinsAC	NP_001729.1:n.-78-4493_-78-4492delinsAC