Canonical Allele Identifier: CA365547679

Gene: MCM9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118856546C>T , CM000668.2:g.118856546C>T	GRCh38
NC_000006.11:g.119177709C>T , CM000668.1:g.119177709C>T	GRCh37
NG_041822.1:g.83617G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_017696.3:c.1151-1G>A MANE Select	NP_060166.2:n.1151-1G>A
ENST00000619706.5:c.1151-1G>A MANE Select	ENSP00000480469.1:n.1151-1G>A
NM_001378356.1:c.1151-1G>A	NP_001365285.1:n.1151-1G>A
NM_001378357.1:c.1151-1G>A	NP_001365286.1:n.1151-1G>A
NM_001378359.1:c.1151-1G>A	NP_001365288.1:n.1151-1G>A
NM_001378360.1:c.1151-1G>A	NP_001365289.1:n.1151-1G>A
NM_001378364.1:c.1151-1G>A	NP_001365293.1:n.1151-1G>A
NM_001378366.1:c.1025-1G>A	NP_001365295.1:n.1025-1G>A
NM_001378367.1:c.953-1G>A	NP_001365296.1:n.953-1G>A
NM_017696.2:c.1151-1G>A	NP_060166.2:n.1151-1G>A
NR_165493.1:n.1435-27296G>A
ENST00000316316.10:c.1151-1G>A	ENSP00000314505.5:n.1151-1G>A
ENST00000368478.2:n.247-27296G>A
ENST00000505485.1:n.331-1G>A
ENST00000619706.4:c.1151-1G>A	ENSP00000480469.1:n.1151-1G>A