Canonical Allele Identifier: CA1658313032

Gene: MCM9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118827834A= , CM000668.2:g.118827834A=	GRCh38
NC_000006.11:g.119148997A= , CM000668.1:g.119148997A=	GRCh37
NC_000006.10:g.119255689A=	NCBI36
NG_041822.1:g.112329T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000619706.5:c.1732+93T= MANE Select	ENSP00000480469.1:n.1732+93T=
ENST00000316316.10:c.1732+93T=	ENSP00000314505.5:n.1732+93T=
ENST00000458674.2:c.207-970T=
ENST00000619706.4:c.1732+93T=	ENSP00000480469.1:n.1732+93T=
NM_017696.2:c.1732+93T=	NP_060166.2:n.1732+93T=
NM_001378356.1:c.1732+93T=	NP_001365285.1:n.1732+93T=
NM_001378357.1:c.1732+93T=	NP_001365286.1:n.1732+93T=
NM_001378359.1:c.1732+93T=	NP_001365288.1:n.1732+93T=
NM_001378360.1:c.1732+93T=	NP_001365289.1:n.1732+93T=
NM_001378364.1:c.1529-970T=	NP_001365293.1:n.1529-970T=
NM_001378366.1:c.1606+93T=	NP_001365295.1:n.1606+93T=
NM_001378367.1:c.1534+93T=	NP_001365296.1:n.1534+93T=
NM_017696.3:c.1732+93T= MANE Select	NP_060166.2:n.1732+93T=
NR_165493.1:n.1841+93T=