Canonical Allele Identifier: CA415858592

Gene: CA6

Linked Data

• MyVariant Identifiers: chr1:g.9017224C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957165C>G , CM000663.2:g.8957165C>G	GRCh38
NC_000001.10:g.9017224C>G , CM000663.1:g.9017224C>G	GRCh37
NC_000001.9:g.8939811C>G	NCBI36
NG_033975.1:g.16332C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.288C>G MANE Select	ENSP00000366662.2:p.Arg96=
ENST00000377436.6:c.288C>G	ENSP00000366654.3:p.Arg96=
ENST00000377442.3:c.108C>G	ENSP00000366661.2:p.Arg36=
ENST00000377443.6:c.288C>G	ENSP00000366662.2:p.Arg96=
ENST00000476083.1:n.99-1745C>G
ENST00000549778.5:c.192C>G	ENSP00000447108.1:p.Arg64=
NM_001215.3:c.288C>G	NP_001206.2:p.Arg96=
NM_001270500.1:c.288C>G	NP_001257429.1:p.Arg96=
NM_001270501.1:c.108C>G	NP_001257430.1:p.Arg36=
NM_001270502.1:c.25-1745C>G	NP_001257431.1:n.25-1745C>G
XM_011542083.1:c.300C>G	XP_011540385.1:p.Arg100=
XM_011542084.1:c.300C>G	XP_011540386.1:p.Arg100=
XM_011542083.3:c.300C>G	XP_011540385.1:p.Arg100=
XM_011542084.3:c.300C>G	XP_011540386.1:p.Arg100=
NM_001215.4:c.288C>G MANE Select	NP_001206.2:p.Arg96=
NM_001270500.2:c.288C>G	NP_001257429.1:p.Arg96=
NM_001270501.2:c.108C>G	NP_001257430.1:p.Arg36=
NM_001270502.2:c.25-1745C>G	NP_001257431.1:n.25-1745C>G