Canonical Allele Identifier: CA415858640

Gene: CA6

Linked Data

• MyVariant Identifiers: chr1:g.9017233G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957174G>T , CM000663.2:g.8957174G>T	GRCh38
NC_000001.10:g.9017233G>T , CM000663.1:g.9017233G>T	GRCh37
NC_000001.9:g.8939820G>T	NCBI36
NG_033975.1:g.16341G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.297G>T MANE Select	ENSP00000366662.2:p.Val99=
ENST00000377436.6:c.297G>T	ENSP00000366654.3:p.Val99=
ENST00000377442.3:c.117G>T	ENSP00000366661.2:p.Val39=
ENST00000377443.6:c.297G>T	ENSP00000366662.2:p.Val99=
ENST00000476083.1:n.99-1736G>T
ENST00000549778.5:c.201G>T	ENSP00000447108.1:p.Val67=
NM_001215.3:c.297G>T	NP_001206.2:p.Val99=
NM_001270500.1:c.297G>T	NP_001257429.1:p.Val99=
NM_001270501.1:c.117G>T	NP_001257430.1:p.Val39=
NM_001270502.1:c.25-1736G>T	NP_001257431.1:n.25-1736G>T
XM_011542083.1:c.309G>T	XP_011540385.1:p.Val103=
XM_011542084.1:c.309G>T	XP_011540386.1:p.Val103=
XM_011542083.3:c.309G>T	XP_011540385.1:p.Val103=
XM_011542084.3:c.309G>T	XP_011540386.1:p.Val103=
NM_001215.4:c.297G>T MANE Select	NP_001206.2:p.Val99=
NM_001270500.2:c.297G>T	NP_001257429.1:p.Val99=
NM_001270501.2:c.117G>T	NP_001257430.1:p.Val39=
NM_001270502.2:c.25-1736G>T	NP_001257431.1:n.25-1736G>T