Canonical Allele Identifier: CA1763804030

Gene: MTMR9

Linked Data

• dbSNP Id: rs2164273

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11310990A>C , CM000670.2:g.11310990A>C	GRCh38
NC_000008.10:g.11168499A>C , CM000670.1:g.11168499A>C	GRCh37
NC_000008.9:g.11205909A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000221086.8:c.971+1302A>C MANE Select	ENSP00000221086.3:n.971+1302A>C
ENST00000221086.7:c.971+1302A>C	ENSP00000221086.3:n.971+1302A>C
ENST00000526292.1:c.716+1302A>C	ENSP00000433239.1:n.716+1302A>C
ENST00000530200.1:c.*717+1302A>C	ENSP00000436046.1:n.*717+1302A>C
NM_015458.3:c.971+1302A>C	NP_056273.2:n.971+1302A>C
XM_011543830.1:c.650+1302A>C	XP_011542132.1:n.650+1302A>C
XM_011543831.1:c.383+1302A>C	XP_011542133.1:n.383+1302A>C
XM_011543830.3:c.650+1302A>C	XP_011542132.1:n.650+1302A>C
XM_011543831.2:c.383+1302A>C	XP_011542133.1:n.383+1302A>C
XM_017013753.2:c.971+1302A>C	XP_016869242.1:n.971+1302A>C
NM_015458.4:c.971+1302A>C MANE Select	NP_056273.2:n.971+1302A>C