Canonical Allele Identifier: CA1152580696

Gene: CA6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957170C= , CM000663.2:g.8957170C=	GRCh38
NC_000001.10:g.9017229C= , CM000663.1:g.9017229C=	GRCh37
NC_000001.9:g.8939816C=	NCBI36
NG_033975.1:g.16337C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.293C= MANE Select	ENSP00000366662.2:p.Thr98=
ENST00000377436.6:c.293C=	ENSP00000366654.3:p.Thr98=
ENST00000377442.3:c.113C=	ENSP00000366661.2:p.Thr38=
ENST00000377443.6:c.293C=	ENSP00000366662.2:p.Thr98=
ENST00000476083.1:n.99-1740C=
ENST00000549778.5:c.197C=	ENSP00000447108.1:p.Thr66=
NM_001215.3:c.293C=	NP_001206.2:p.Thr98=
NM_001270500.1:c.293C=	NP_001257429.1:p.Thr98=
NM_001270501.1:c.113C=	NP_001257430.1:p.Thr38=
NM_001270502.1:c.25-1740C=	NP_001257431.1:n.25-1740C=
XM_011542083.1:c.305C=	XP_011540385.1:p.Thr102=
XM_011542084.1:c.305C=	XP_011540386.1:p.Thr102=
XM_011542083.3:c.305C=	XP_011540385.1:p.Thr102=
XM_011542084.3:c.305C=	XP_011540386.1:p.Thr102=
NM_001215.4:c.293C= MANE Select	NP_001206.2:p.Thr98=
NM_001270500.2:c.293C=	NP_001257429.1:p.Thr98=
NM_001270501.2:c.113C=	NP_001257430.1:p.Thr38=
NM_001270502.2:c.25-1740C=	NP_001257431.1:n.25-1740C=