Canonical Allele Identifier: CA365466441

Gene: MCM9

Linked Data

• MyVariant Identifiers: chr6:g.119245164A>C (hg19) ; chr6:g.118923999A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118923999A>C , CM000668.2:g.118923999A>C	GRCh38
NC_000006.11:g.119245164A>C , CM000668.1:g.119245164A>C	GRCh37
NC_000006.10:g.119286863A>C	NCBI36
NG_041822.1:g.16164T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619706.5:c.433T>G MANE Select	ENSP00000480469.1:p.Tyr145Asp
ENST00000316068.7:c.433T>G	ENSP00000312870.3:p.Tyr145Asp
ENST00000316316.10:c.433T>G	ENSP00000314505.5:p.Tyr145Asp
ENST00000425154.6:c.433T>G	ENSP00000394776.2:p.Tyr145Asp
ENST00000436788.2:n.54T>G
ENST00000619706.4:c.433T>G	ENSP00000480469.1:p.Tyr145Asp
NM_017696.2:c.433T>G	NP_060166.2:p.Tyr145Asp
NM_153255.4:c.433T>G	NP_694987.1:p.Tyr145Asp
NM_001378356.1:c.433T>G	NP_001365285.1:p.Tyr145Asp
NM_001378357.1:c.433T>G	NP_001365286.1:p.Tyr145Asp
NM_001378358.1:c.433T>G	NP_001365287.1:p.Tyr145Asp
NM_001378359.1:c.433T>G	NP_001365288.1:p.Tyr145Asp
NM_001378360.1:c.433T>G	NP_001365289.1:p.Tyr145Asp
NM_001378361.1:c.235T>G	NP_001365290.1:p.Tyr79Asp
NM_001378362.1:c.235T>G	NP_001365291.1:p.Tyr79Asp
NM_001378363.1:c.235T>G	NP_001365292.1:p.Tyr79Asp
NM_001378364.1:c.433T>G	NP_001365293.1:p.Tyr145Asp
NM_001378365.1:c.433T>G	NP_001365294.1:p.Tyr145Asp
NM_001378366.1:c.433T>G	NP_001365295.1:p.Tyr145Asp
NM_001378367.1:c.235T>G	NP_001365296.1:p.Tyr79Asp
NM_001378368.1:c.433T>G	NP_001365297.1:p.Tyr145Asp
NM_001378369.1:c.433T>G	NP_001365298.1:p.Tyr145Asp
NM_001378370.1:c.235T>G	NP_001365299.1:p.Tyr79Asp
NM_001378371.1:c.433T>G	NP_001365300.1:p.Tyr145Asp
NM_001378372.1:c.235T>G	NP_001365301.1:p.Tyr79Asp
NM_017696.3:c.433T>G MANE Select	NP_060166.2:p.Tyr145Asp
NM_153255.5:c.433T>G	NP_694987.1:p.Tyr145Asp
NR_165493.1:n.717T>G
NR_165494.1:n.851T>G