Canonical Allele Identifier: CA461785639

Gene: CA1

Linked Data

• MyVariant Identifiers: chr8:g.86240822A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.85328593A>T , CM000670.2:g.85328593A>T	GRCh38
NC_000008.10:g.86240822A>T , CM000670.1:g.86240822A>T	GRCh37
NC_000008.9:g.86428074A>T	NCBI36
NG_016221.1:g.54521T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523022.6:c.753T>A MANE Select	ENSP00000429798.1:p.Pro251=
ENST00000431316.3:c.753T>A	ENSP00000392338.1:p.Pro251=
ENST00000517618.5:c.753T>A	ENSP00000430861.1:p.Pro251=
ENST00000521679.5:c.502T>A
ENST00000522389.5:c.351T>A	ENSP00000427773.1:p.Pro117=
ENST00000523022.5:c.753T>A	ENSP00000429798.1:p.Pro251=
ENST00000523953.5:c.753T>A	ENSP00000430656.1:p.Pro251=
ENST00000524324.5:c.555T>A	ENSP00000428923.1:p.Pro185=
ENST00000542576.5:c.753T>A	ENSP00000443517.1:p.Pro251=
ENST00000626824.1:c.351T>A	ENSP00000486171.1:p.Pro117=
NM_001128829.3:c.753T>A	NP_001122301.1:p.Pro251=
NM_001128830.3:c.753T>A	NP_001122302.1:p.Pro251=
NM_001128831.3:c.753T>A	NP_001122303.1:p.Pro251=
NM_001164830.1:c.753T>A	NP_001158302.1:p.Pro251=
NM_001291967.1:c.555T>A	NP_001278896.1:p.Pro185=
NM_001291968.1:c.414T>A	NP_001278897.1:p.Pro138=
NM_001738.4:c.753T>A	NP_001729.1:p.Pro251=
XM_011517584.1:c.753T>A	XP_011515886.1:p.Pro251=
NM_001128829.4:c.753T>A	NP_001122301.1:p.Pro251=
NM_001128830.4:c.753T>A	NP_001122302.1:p.Pro251=
NM_001128831.4:c.753T>A MANE Select	NP_001122303.1:p.Pro251=
NM_001164830.2:c.753T>A	NP_001158302.1:p.Pro251=
NM_001291967.2:c.555T>A	NP_001278896.1:p.Pro185=
NM_001291968.2:c.414T>A	NP_001278897.1:p.Pro138=
NM_001738.5:c.753T>A	NP_001729.1:p.Pro251=