Canonical Allele Identifier: CA365550914

Gene: MCM9

Linked Data

• MyVariant Identifiers: chr6:g.119149095G>T (hg19) ; chr6:g.118827932G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118827932G>T , CM000668.2:g.118827932G>T	GRCh38
NC_000006.11:g.119149095G>T , CM000668.1:g.119149095G>T	GRCh37
NC_000006.10:g.119255787G>T	NCBI36
NG_041822.1:g.112231C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619706.5:c.1727C>A MANE Select	ENSP00000480469.1:p.Ala576Glu
ENST00000316316.10:c.1727C>A	ENSP00000314505.5:p.Ala576Glu
ENST00000458674.2:c.207-1068C>A
ENST00000619706.4:c.1727C>A	ENSP00000480469.1:p.Ala576Glu
NM_017696.2:c.1727C>A	NP_060166.2:p.Ala576Glu
NM_001378356.1:c.1727C>A	NP_001365285.1:p.Ala576Glu
NM_001378357.1:c.1727C>A	NP_001365286.1:p.Ala576Glu
NM_001378359.1:c.1727C>A	NP_001365288.1:p.Ala576Glu
NM_001378360.1:c.1727C>A	NP_001365289.1:p.Ala576Glu
NM_001378364.1:c.1529-1068C>A	NP_001365293.1:n.1529-1068C>A
NM_001378366.1:c.1601C>A	NP_001365295.1:p.Ala534Glu
NM_001378367.1:c.1529C>A	NP_001365296.1:p.Ala510Glu
NM_017696.3:c.1727C>A MANE Select	NP_060166.2:p.Ala576Glu
NR_165493.1:n.1836C>A