Canonical Allele Identifier: CA371418526

Gene: CA1

Linked Data

• MyVariant Identifiers: chr8:g.86240823G>C (hg19) ; chr8:g.85328594G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.85328594G>C , CM000670.2:g.85328594G>C	GRCh38
NC_000008.10:g.86240823G>C , CM000670.1:g.86240823G>C	GRCh37
NC_000008.9:g.86428075G>C	NCBI36
NG_016221.1:g.54520C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523022.6:c.752C>G MANE Select	ENSP00000429798.1:p.Pro251Arg
ENST00000431316.3:c.752C>G	ENSP00000392338.1:p.Pro251Arg
ENST00000517618.5:c.752C>G	ENSP00000430861.1:p.Pro251Arg
ENST00000519991.5:c.413C>G
ENST00000521679.5:c.501C>G
ENST00000522389.5:c.350C>G	ENSP00000427773.1:p.Pro117Arg
ENST00000523022.5:c.752C>G	ENSP00000429798.1:p.Pro251Arg
ENST00000523953.5:c.752C>G	ENSP00000430656.1:p.Pro251Arg
ENST00000524324.5:c.554C>G	ENSP00000428923.1:p.Pro185Arg
ENST00000542576.5:c.752C>G	ENSP00000443517.1:p.Pro251Arg
ENST00000626824.1:c.350C>G	ENSP00000486171.1:p.Pro117Arg
NM_001128829.3:c.752C>G	NP_001122301.1:p.Pro251Arg
NM_001128830.3:c.752C>G	NP_001122302.1:p.Pro251Arg
NM_001128831.3:c.752C>G	NP_001122303.1:p.Pro251Arg
NM_001164830.1:c.752C>G	NP_001158302.1:p.Pro251Arg
NM_001291967.1:c.554C>G	NP_001278896.1:p.Pro185Arg
NM_001291968.1:c.413C>G	NP_001278897.1:p.Pro138Arg
NM_001738.4:c.752C>G	NP_001729.1:p.Pro251Arg
XM_011517584.1:c.752C>G	XP_011515886.1:p.Pro251Arg
NM_001128829.4:c.752C>G	NP_001122301.1:p.Pro251Arg
NM_001128830.4:c.752C>G	NP_001122302.1:p.Pro251Arg
NM_001128831.4:c.752C>G MANE Select	NP_001122303.1:p.Pro251Arg
NM_001164830.2:c.752C>G	NP_001158302.1:p.Pro251Arg
NM_001291967.2:c.554C>G	NP_001278896.1:p.Pro185Arg
NM_001291968.2:c.413C>G	NP_001278897.1:p.Pro138Arg
NM_001738.5:c.752C>G	NP_001729.1:p.Pro251Arg