Canonical Allele Identifier: CA415858902

Gene: CA6

Linked Data

• MyVariant Identifiers: chr1:g.9017305C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957246C>G , CM000663.2:g.8957246C>G	GRCh38
NC_000001.10:g.9017305C>G , CM000663.1:g.9017305C>G	GRCh37
NC_000001.9:g.8939892C>G	NCBI36
NG_033975.1:g.16413C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.369C>G MANE Select	ENSP00000366662.2:p.Gly123=
ENST00000377436.6:c.369C>G	ENSP00000366654.3:p.Gly123=
ENST00000377442.3:c.189C>G	ENSP00000366661.2:p.Gly63=
ENST00000377443.6:c.369C>G	ENSP00000366662.2:p.Gly123=
ENST00000476083.1:n.99-1664C>G
ENST00000549778.5:c.273C>G	ENSP00000447108.1:p.Gly91=
NM_001215.3:c.369C>G	NP_001206.2:p.Gly123=
NM_001270500.1:c.369C>G	NP_001257429.1:p.Gly123=
NM_001270501.1:c.189C>G	NP_001257430.1:p.Gly63=
NM_001270502.1:c.25-1664C>G	NP_001257431.1:n.25-1664C>G
XM_011542083.1:c.381C>G	XP_011540385.1:p.Gly127=
XM_011542084.1:c.381C>G	XP_011540386.1:p.Gly127=
XM_011542083.3:c.381C>G	XP_011540385.1:p.Gly127=
XM_011542084.3:c.381C>G	XP_011540386.1:p.Gly127=
NM_001215.4:c.369C>G MANE Select	NP_001206.2:p.Gly123=
NM_001270500.2:c.369C>G	NP_001257429.1:p.Gly123=
NM_001270501.2:c.189C>G	NP_001257430.1:p.Gly63=
NM_001270502.2:c.25-1664C>G	NP_001257431.1:n.25-1664C>G