Canonical Allele Identifier: CA1799299557

Gene: CA1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.85356145_85356146delinsAT , CM000670.2:g.85356145_85356146delinsAT	GRCh38
NC_000008.10:g.86268374_86268375delinsAT , CM000670.1:g.86268374_86268375delinsAT	GRCh37
NC_000008.9:g.86455626_86455627delinsAT	NCBI36
NG_016221.1:g.26968_26969delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000523022.6:c.-24-14487_-24-14486delinsAT MANE Select	ENSP00000429798.1:n.-24-14487_-24-14486delinsAT
ENST00000517429.5:c.-24-14487_-24-14486delinsAT	ENSP00000430710.1:n.-24-14487_-24-14486delinsAT
ENST00000517590.5:c.-101-13321_-101-13320delinsAT	ENSP00000429843.1:n.-101-13321_-101-13320delinsAT
ENST00000518341.5:n.69-14487_69-14486delinsAT
ENST00000519129.5:c.-356-4362_-356-4361delinsAT	ENSP00000429688.1:n.-356-4362_-356-4361delinsAT
ENST00000519991.5:c.-46-14487_-46-14486delinsAT	ENSP00000430543.1:n.-46-14487_-46-14486delinsAT
ENST00000520093.5:n.69-14487_69-14486delinsAT
ENST00000520663.5:c.-123-13321_-123-13320delinsAT	ENSP00000430571.1:n.-123-13321_-123-13320delinsAT
ENST00000520990.5:n.69-13321_69-13320delinsAT
ENST00000521846.5:c.-155-4362_-155-4361delinsAT	ENSP00000430471.1:n.-155-4362_-155-4361delinsAT
ENST00000522579.5:c.-99-6261_-99-6260delinsAT	ENSP00000427852.1:n.-99-6261_-99-6260delinsAT
ENST00000522662.5:c.-79-14338_-79-14337delinsAT	ENSP00000430372.1:n.-79-14338_-79-14337delinsAT
ENST00000522814.5:c.-105-14312_-105-14311delinsAT	ENSP00000430737.1:n.-105-14312_-105-14311delinsAT
ENST00000523022.5:c.-24-14487_-24-14486delinsAT	ENSP00000429798.1:n.-24-14487_-24-14486delinsAT
ENST00000523858.5:c.-153-4362_-153-4361delinsAT	ENSP00000430975.1:n.-153-4362_-153-4361delinsAT
ENST00000523953.5:c.-78-4362_-78-4361delinsAT	ENSP00000430656.1:n.-78-4362_-78-4361delinsAT
ENST00000524324.5:c.-24-14487_-24-14486delinsAT	ENSP00000428923.1:n.-24-14487_-24-14486delinsAT
ENST00000626824.1:c.-100-4362_-100-4361delinsAT	ENSP00000486171.1:n.-100-4362_-100-4361delinsAT
NM_001128829.3:c.-99-6261_-99-6260delinsAT	NP_001122301.1:n.-99-6261_-99-6260delinsAT
NM_001128830.3:c.-101-13321_-101-13320delinsAT	NP_001122302.1:n.-101-13321_-101-13320delinsAT
NM_001128831.3:c.-24-14487_-24-14486delinsAT	NP_001122303.1:n.-24-14487_-24-14486delinsAT
NM_001291967.1:c.-24-14487_-24-14486delinsAT	NP_001278896.1:n.-24-14487_-24-14486delinsAT
NM_001291968.1:c.-46-14487_-46-14486delinsAT	NP_001278897.1:n.-46-14487_-46-14486delinsAT
NM_001738.4:c.-78-4362_-78-4361delinsAT	NP_001729.1:n.-78-4362_-78-4361delinsAT
XM_011517584.1:c.-155-4362_-155-4361delinsAT	XP_011515886.1:n.-155-4362_-155-4361delinsAT
NM_001128829.4:c.-99-6261_-99-6260delinsAT	NP_001122301.1:n.-99-6261_-99-6260delinsAT
NM_001128830.4:c.-101-13321_-101-13320delinsAT	NP_001122302.1:n.-101-13321_-101-13320delinsAT
NM_001128831.4:c.-24-14487_-24-14486delinsAT MANE Select	NP_001122303.1:n.-24-14487_-24-14486delinsAT
NM_001291967.2:c.-24-14487_-24-14486delinsAT	NP_001278896.1:n.-24-14487_-24-14486delinsAT
NM_001291968.2:c.-46-14487_-46-14486delinsAT	NP_001278897.1:n.-46-14487_-46-14486delinsAT
NM_001738.5:c.-78-4362_-78-4361delinsAT	NP_001729.1:n.-78-4362_-78-4361delinsAT