Canonical Allele Identifier: CA415858904

Gene: CA6

Linked Data

• MyVariant Identifiers: chr1:g.9017308T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957249T>G , CM000663.2:g.8957249T>G	GRCh38
NC_000001.10:g.9017308T>G , CM000663.1:g.9017308T>G	GRCh37
NC_000001.9:g.8939895T>G	NCBI36
NG_033975.1:g.16416T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.372T>G MANE Select	ENSP00000366662.2:p.Ser124=
ENST00000377436.6:c.372T>G	ENSP00000366654.3:p.Ser124=
ENST00000377442.3:c.192T>G	ENSP00000366661.2:p.Ser64=
ENST00000377443.6:c.372T>G	ENSP00000366662.2:p.Ser124=
ENST00000476083.1:n.99-1661T>G
ENST00000549778.5:c.276T>G	ENSP00000447108.1:p.Ser92=
NM_001215.3:c.372T>G	NP_001206.2:p.Ser124=
NM_001270500.1:c.372T>G	NP_001257429.1:p.Ser124=
NM_001270501.1:c.192T>G	NP_001257430.1:p.Ser64=
NM_001270502.1:c.25-1661T>G	NP_001257431.1:n.25-1661T>G
XM_011542083.1:c.384T>G	XP_011540385.1:p.Ser128=
XM_011542084.1:c.384T>G	XP_011540386.1:p.Ser128=
XM_011542083.3:c.384T>G	XP_011540385.1:p.Ser128=
XM_011542084.3:c.384T>G	XP_011540386.1:p.Ser128=
NM_001215.4:c.372T>G MANE Select	NP_001206.2:p.Ser124=
NM_001270500.2:c.372T>G	NP_001257429.1:p.Ser124=
NM_001270501.2:c.192T>G	NP_001257430.1:p.Ser64=
NM_001270502.2:c.25-1661T>G	NP_001257431.1:n.25-1661T>G