Canonical Allele Identifier: CA365550931

Gene: MCM9

Linked Data

• MyVariant Identifiers: chr6:g.119149104A>G (hg19) ; chr6:g.118827941A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118827941A>G , CM000668.2:g.118827941A>G	GRCh38
NC_000006.11:g.119149104A>G , CM000668.1:g.119149104A>G	GRCh37
NC_000006.10:g.119255796A>G	NCBI36
NG_041822.1:g.112222T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619706.5:c.1718T>C MANE Select	ENSP00000480469.1:p.Ile573Thr
ENST00000316316.10:c.1718T>C	ENSP00000314505.5:p.Ile573Thr
ENST00000458674.2:c.207-1077T>C
ENST00000619706.4:c.1718T>C	ENSP00000480469.1:p.Ile573Thr
NM_017696.2:c.1718T>C	NP_060166.2:p.Ile573Thr
NM_001378356.1:c.1718T>C	NP_001365285.1:p.Ile573Thr
NM_001378357.1:c.1718T>C	NP_001365286.1:p.Ile573Thr
NM_001378359.1:c.1718T>C	NP_001365288.1:p.Ile573Thr
NM_001378360.1:c.1718T>C	NP_001365289.1:p.Ile573Thr
NM_001378364.1:c.1529-1077T>C	NP_001365293.1:n.1529-1077T>C
NM_001378366.1:c.1592T>C	NP_001365295.1:p.Ile531Thr
NM_001378367.1:c.1520T>C	NP_001365296.1:p.Ile507Thr
NM_017696.3:c.1718T>C MANE Select	NP_060166.2:p.Ile573Thr
NR_165493.1:n.1827T>C