Canonical Allele Identifier: CA371418373

Gene: CA1

Linked Data

• MyVariant Identifiers: chr8:g.86240793A>C (hg19) ; chr8:g.85328564A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.85328564A>C , CM000670.2:g.85328564A>C	GRCh38
NC_000008.10:g.86240793A>C , CM000670.1:g.86240793A>C	GRCh37
NC_000008.9:g.86428045A>C	NCBI36
NG_016221.1:g.54550T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523022.6:c.782T>G MANE Select	ENSP00000429798.1:p.Phe261Cys
ENST00000431316.3:c.782T>G	ENSP00000392338.1:p.Phe261Cys
ENST00000521679.5:c.531T>G
ENST00000522389.5:c.380T>G	ENSP00000427773.1:p.Phe127Cys
ENST00000523022.5:c.782T>G	ENSP00000429798.1:p.Phe261Cys
ENST00000523953.5:c.782T>G	ENSP00000430656.1:p.Phe261Cys
ENST00000542576.5:c.782T>G	ENSP00000443517.1:p.Phe261Cys
ENST00000626824.1:c.380T>G	ENSP00000486171.1:p.Phe127Cys
NM_001128829.3:c.782T>G	NP_001122301.1:p.Phe261Cys
NM_001128830.3:c.782T>G	NP_001122302.1:p.Phe261Cys
NM_001128831.3:c.782T>G	NP_001122303.1:p.Phe261Cys
NM_001164830.1:c.782T>G	NP_001158302.1:p.Phe261Cys
NM_001291967.1:c.584T>G	NP_001278896.1:p.Phe195Cys
NM_001291968.1:c.443T>G	NP_001278897.1:p.Phe148Cys
NM_001738.4:c.782T>G	NP_001729.1:p.Phe261Cys
XM_011517584.1:c.782T>G	XP_011515886.1:p.Phe261Cys
NM_001128829.4:c.782T>G	NP_001122301.1:p.Phe261Cys
NM_001128830.4:c.782T>G	NP_001122302.1:p.Phe261Cys
NM_001128831.4:c.782T>G MANE Select	NP_001122303.1:p.Phe261Cys
NM_001164830.2:c.782T>G	NP_001158302.1:p.Phe261Cys
NM_001291967.2:c.584T>G	NP_001278896.1:p.Phe195Cys
NM_001291968.2:c.443T>G	NP_001278897.1:p.Phe148Cys
NM_001738.5:c.782T>G	NP_001729.1:p.Phe261Cys