Canonical Allele Identifier: CA1658312955

Gene: MCM9

Linked Data

• dbSNP Id: rs1774252891

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118827673_118827674insCAAATGTAAA , CM000668.2:g.118827673_118827674insCAAATGTAAA	GRCh38
NC_000006.11:g.119148836_119148837insCAAATGTAAA , CM000668.1:g.119148836_119148837insCAAATGTAAA	GRCh37
NC_000006.10:g.119255528_119255529insCAAATGTAAA	NCBI36
NG_041822.1:g.112489_112490insTTTACATTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619706.5:c.1732+253_1732+254insTTTACATTTG MANE Select	ENSP00000480469.1:n.1732+253_1732+254insTTTACATTTG
ENST00000316316.10:c.1732+253_1732+254insTTTACATTTG	ENSP00000314505.5:n.1732+253_1732+254insTTTACATTTG
ENST00000458674.2:c.207-810_207-809insTTTACATTTG
ENST00000619706.4:c.1732+253_1732+254insTTTACATTTG	ENSP00000480469.1:n.1732+253_1732+254insTTTACATTTG
NM_017696.2:c.1732+253_1732+254insTTTACATTTG	NP_060166.2:n.1732+253_1732+254insTTTACATTTG
NM_001378356.1:c.1732+253_1732+254insTTTACATTTG	NP_001365285.1:n.1732+253_1732+254insTTTACATTTG
NM_001378357.1:c.1732+253_1732+254insTTTACATTTG	NP_001365286.1:n.1732+253_1732+254insTTTACATTTG
NM_001378359.1:c.1732+253_1732+254insTTTACATTTG	NP_001365288.1:n.1732+253_1732+254insTTTACATTTG
NM_001378360.1:c.1732+253_1732+254insTTTACATTTG	NP_001365289.1:n.1732+253_1732+254insTTTACATTTG
NM_001378364.1:c.1529-810_1529-809insTTTACATTTG	NP_001365293.1:n.1529-810_1529-809insTTTACATTTG
NM_001378366.1:c.1606+253_1606+254insTTTACATTTG	NP_001365295.1:n.1606+253_1606+254insTTTACATTTG
NM_001378367.1:c.1534+253_1534+254insTTTACATTTG	NP_001365296.1:n.1534+253_1534+254insTTTACATTTG
NM_017696.3:c.1732+253_1732+254insTTTACATTTG MANE Select	NP_060166.2:n.1732+253_1732+254insTTTACATTTG
NR_165493.1:n.1841+253_1841+254insTTTACATTTG