Canonical Allele Identifier: CA452026186

Gene: MCM9

Linked Data

• MyVariant Identifiers: chr6:g.119149094T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118827931T>A , CM000668.2:g.118827931T>A	GRCh38
NC_000006.11:g.119149094T>A , CM000668.1:g.119149094T>A	GRCh37
NC_000006.10:g.119255786T>A	NCBI36
NG_041822.1:g.112232A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619706.5:c.1728A>T MANE Select	ENSP00000480469.1:p.Ala576=
ENST00000316316.10:c.1728A>T	ENSP00000314505.5:p.Ala576=
ENST00000458674.2:c.207-1067A>T
ENST00000619706.4:c.1728A>T	ENSP00000480469.1:p.Ala576=
NM_017696.2:c.1728A>T	NP_060166.2:p.Ala576=
NM_001378356.1:c.1728A>T	NP_001365285.1:p.Ala576=
NM_001378357.1:c.1728A>T	NP_001365286.1:p.Ala576=
NM_001378359.1:c.1728A>T	NP_001365288.1:p.Ala576=
NM_001378360.1:c.1728A>T	NP_001365289.1:p.Ala576=
NM_001378364.1:c.1529-1067A>T	NP_001365293.1:n.1529-1067A>T
NM_001378366.1:c.1602A>T	NP_001365295.1:p.Ala534=
NM_001378367.1:c.1530A>T	NP_001365296.1:p.Ala510=
NM_017696.3:c.1728A>T MANE Select	NP_060166.2:p.Ala576=
NR_165493.1:n.1837A>T