Canonical Allele Identifier: CA1152580848

Gene: CA6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957275A= , CM000663.2:g.8957275A=	GRCh38
NC_000001.10:g.9017334A= , CM000663.1:g.9017334A=	GRCh37
NC_000001.9:g.8939921A=	NCBI36
NG_033975.1:g.16442A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.398A= MANE Select	ENSP00000366662.2:p.His133=
ENST00000377436.6:c.398A=	ENSP00000366654.3:p.His133=
ENST00000377442.3:c.218A=	ENSP00000366661.2:p.His73=
ENST00000377443.6:c.398A=	ENSP00000366662.2:p.His133=
ENST00000476083.1:n.99-1635A=
ENST00000549778.5:c.302A=	ENSP00000447108.1:p.His101=
NM_001215.3:c.398A=	NP_001206.2:p.His133=
NM_001270500.1:c.398A=	NP_001257429.1:p.His133=
NM_001270501.1:c.218A=	NP_001257430.1:p.His73=
NM_001270502.1:c.25-1635A=	NP_001257431.1:n.25-1635A=
XM_011542083.1:c.410A=	XP_011540385.1:p.His137=
XM_011542084.1:c.410A=	XP_011540386.1:p.His137=
XM_011542083.3:c.410A=	XP_011540385.1:p.His137=
XM_011542084.3:c.410A=	XP_011540386.1:p.His137=
NM_001215.4:c.398A= MANE Select	NP_001206.2:p.His133=
NM_001270500.2:c.398A=	NP_001257429.1:p.His133=
NM_001270501.2:c.218A=	NP_001257430.1:p.His73=
NM_001270502.2:c.25-1635A=	NP_001257431.1:n.25-1635A=