Canonical Allele Identifier: CA2680169145

Gene: MCM9

Linked Data

• gnomAD v4: 6-118827839-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118827839C>A , CM000668.2:g.118827839C>A	GRCh38
NC_000006.11:g.119149002C>A , CM000668.1:g.119149002C>A	GRCh37
NC_000006.10:g.119255694C>A	NCBI36
NG_041822.1:g.112324G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619706.5:c.1732+88G>T MANE Select	ENSP00000480469.1:n.1732+88G>T
ENST00000316316.10:c.1732+88G>T	ENSP00000314505.5:n.1732+88G>T
ENST00000458674.2:c.207-975G>T
ENST00000619706.4:c.1732+88G>T	ENSP00000480469.1:n.1732+88G>T
NM_017696.2:c.1732+88G>T	NP_060166.2:n.1732+88G>T
NM_001378356.1:c.1732+88G>T	NP_001365285.1:n.1732+88G>T
NM_001378357.1:c.1732+88G>T	NP_001365286.1:n.1732+88G>T
NM_001378359.1:c.1732+88G>T	NP_001365288.1:n.1732+88G>T
NM_001378360.1:c.1732+88G>T	NP_001365289.1:n.1732+88G>T
NM_001378364.1:c.1529-975G>T	NP_001365293.1:n.1529-975G>T
NM_001378366.1:c.1606+88G>T	NP_001365295.1:n.1606+88G>T
NM_001378367.1:c.1534+88G>T	NP_001365296.1:n.1534+88G>T
NM_017696.3:c.1732+88G>T MANE Select	NP_060166.2:n.1732+88G>T
NR_165493.1:n.1841+88G>T