Canonical Allele Identifier: CA1152580691

Gene: CA6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957169A= , CM000663.2:g.8957169A=	GRCh38
NC_000001.10:g.9017228A= , CM000663.1:g.9017228A=	GRCh37
NC_000001.9:g.8939815A=	NCBI36
NG_033975.1:g.16336A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.292A= MANE Select	ENSP00000366662.2:p.Thr98=
ENST00000377436.6:c.292A=	ENSP00000366654.3:p.Thr98=
ENST00000377442.3:c.112A=	ENSP00000366661.2:p.Thr38=
ENST00000377443.6:c.292A=	ENSP00000366662.2:p.Thr98=
ENST00000476083.1:n.99-1741A=
ENST00000549778.5:c.196A=	ENSP00000447108.1:p.Thr66=
NM_001215.3:c.292A=	NP_001206.2:p.Thr98=
NM_001270500.1:c.292A=	NP_001257429.1:p.Thr98=
NM_001270501.1:c.112A=	NP_001257430.1:p.Thr38=
NM_001270502.1:c.25-1741A=	NP_001257431.1:n.25-1741A=
XM_011542083.1:c.304A=	XP_011540385.1:p.Thr102=
XM_011542084.1:c.304A=	XP_011540386.1:p.Thr102=
XM_011542083.3:c.304A=	XP_011540385.1:p.Thr102=
XM_011542084.3:c.304A=	XP_011540386.1:p.Thr102=
NM_001215.4:c.292A= MANE Select	NP_001206.2:p.Thr98=
NM_001270500.2:c.292A=	NP_001257429.1:p.Thr98=
NM_001270501.2:c.112A=	NP_001257430.1:p.Thr38=
NM_001270502.2:c.25-1741A=	NP_001257431.1:n.25-1741A=