Canonical Allele Identifier: CA2781117896

Gene: CA1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.85356120_85356125del , CM000670.2:g.85356120_85356125del	GRCh38
NC_000008.10:g.86268349_86268354del , CM000670.1:g.86268349_86268354del	GRCh37
NC_000008.9:g.86455601_86455606del	NCBI36
NG_016221.1:g.26989_26994del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523022.6:c.-24-14466_-24-14461del MANE Select	ENSP00000429798.1:n.-24-14466_-24-14461del
ENST00000517429.5:c.-24-14466_-24-14461del	ENSP00000430710.1:n.-24-14466_-24-14461del
ENST00000517590.5:c.-101-13300_-101-13295del	ENSP00000429843.1:n.-101-13300_-101-13295del
ENST00000518341.5:n.69-14466_69-14461del
ENST00000519129.5:c.-356-4341_-356-4336del	ENSP00000429688.1:n.-356-4341_-356-4336del
ENST00000519991.5:c.-46-14466_-46-14461del	ENSP00000430543.1:n.-46-14466_-46-14461del
ENST00000520093.5:n.69-14466_69-14461del
ENST00000520663.5:c.-123-13300_-123-13295del	ENSP00000430571.1:n.-123-13300_-123-13295del
ENST00000520990.5:n.69-13300_69-13295del
ENST00000521846.5:c.-155-4341_-155-4336del	ENSP00000430471.1:n.-155-4341_-155-4336del
ENST00000522579.5:c.-99-6240_-99-6235del	ENSP00000427852.1:n.-99-6240_-99-6235del
ENST00000522662.5:c.-79-14317_-79-14312del	ENSP00000430372.1:n.-79-14317_-79-14312del
ENST00000522814.5:c.-105-14291_-105-14286del	ENSP00000430737.1:n.-105-14291_-105-14286del
ENST00000523022.5:c.-24-14466_-24-14461del	ENSP00000429798.1:n.-24-14466_-24-14461del
ENST00000523858.5:c.-153-4341_-153-4336del	ENSP00000430975.1:n.-153-4341_-153-4336del
ENST00000523953.5:c.-78-4341_-78-4336del	ENSP00000430656.1:n.-78-4341_-78-4336del
ENST00000524324.5:c.-24-14466_-24-14461del	ENSP00000428923.1:n.-24-14466_-24-14461del
ENST00000626824.1:c.-100-4341_-100-4336del	ENSP00000486171.1:n.-100-4341_-100-4336del
NM_001128829.3:c.-99-6240_-99-6235del	NP_001122301.1:n.-99-6240_-99-6235del
NM_001128830.3:c.-101-13300_-101-13295del	NP_001122302.1:n.-101-13300_-101-13295del
NM_001128831.3:c.-24-14466_-24-14461del	NP_001122303.1:n.-24-14466_-24-14461del
NM_001291967.1:c.-24-14466_-24-14461del	NP_001278896.1:n.-24-14466_-24-14461del
NM_001291968.1:c.-46-14466_-46-14461del	NP_001278897.1:n.-46-14466_-46-14461del
NM_001738.4:c.-78-4341_-78-4336del	NP_001729.1:n.-78-4341_-78-4336del
XM_011517584.1:c.-155-4341_-155-4336del	XP_011515886.1:n.-155-4341_-155-4336del
NM_001128829.4:c.-99-6240_-99-6235del	NP_001122301.1:n.-99-6240_-99-6235del
NM_001128830.4:c.-101-13300_-101-13295del	NP_001122302.1:n.-101-13300_-101-13295del
NM_001128831.4:c.-24-14466_-24-14461del MANE Select	NP_001122303.1:n.-24-14466_-24-14461del
NM_001291967.2:c.-24-14466_-24-14461del	NP_001278896.1:n.-24-14466_-24-14461del
NM_001291968.2:c.-46-14466_-46-14461del	NP_001278897.1:n.-46-14466_-46-14461del
NM_001738.5:c.-78-4341_-78-4336del	NP_001729.1:n.-78-4341_-78-4336del