Canonical Allele Identifier: CA1658313038

Gene: MCM9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118827845A= , CM000668.2:g.118827845A=	GRCh38
NC_000006.11:g.119149008A= , CM000668.1:g.119149008A=	GRCh37
NC_000006.10:g.119255700A=	NCBI36
NG_041822.1:g.112318T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619706.5:c.1732+82T= MANE Select	ENSP00000480469.1:n.1732+82T=
ENST00000316316.10:c.1732+82T=	ENSP00000314505.5:n.1732+82T=
ENST00000458674.2:c.207-981T=
ENST00000619706.4:c.1732+82T=	ENSP00000480469.1:n.1732+82T=
NM_017696.2:c.1732+82T=	NP_060166.2:n.1732+82T=
NM_001378356.1:c.1732+82T=	NP_001365285.1:n.1732+82T=
NM_001378357.1:c.1732+82T=	NP_001365286.1:n.1732+82T=
NM_001378359.1:c.1732+82T=	NP_001365288.1:n.1732+82T=
NM_001378360.1:c.1732+82T=	NP_001365289.1:n.1732+82T=
NM_001378364.1:c.1529-981T=	NP_001365293.1:n.1529-981T=
NM_001378366.1:c.1606+82T=	NP_001365295.1:n.1606+82T=
NM_001378367.1:c.1534+82T=	NP_001365296.1:n.1534+82T=
NM_017696.3:c.1732+82T= MANE Select	NP_060166.2:n.1732+82T=
NR_165493.1:n.1841+82T=