Canonical Allele Identifier: CA365550912

Gene: MCM9

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000619706.5:c.1727C>T MANE Select	ENSP00000480469.1:p.Ala576Val
ENST00000316316.10:c.1727C>T	ENSP00000314505.5:p.Ala576Val
ENST00000458674.2:c.207-1068C>T
ENST00000619706.4:c.1727C>T	ENSP00000480469.1:p.Ala576Val
NM_017696.2:c.1727C>T	NP_060166.2:p.Ala576Val
NM_001378356.1:c.1727C>T	NP_001365285.1:p.Ala576Val
NM_001378357.1:c.1727C>T	NP_001365286.1:p.Ala576Val
NM_001378359.1:c.1727C>T	NP_001365288.1:p.Ala576Val
NM_001378360.1:c.1727C>T	NP_001365289.1:p.Ala576Val
NM_001378364.1:c.1529-1068C>T	NP_001365293.1:n.1529-1068C>T
NM_001378366.1:c.1601C>T	NP_001365295.1:p.Ala534Val
NM_001378367.1:c.1529C>T	NP_001365296.1:p.Ala510Val
NM_017696.3:c.1727C>T MANE Select	NP_060166.2:p.Ala576Val
NR_165493.1:n.1836C>T