Canonical Allele Identifier: CA2729691608

Gene: MAP3K9

Linked Data

• dbSNP Id: rs2139688054

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.70727468C>G , CM000676.2:g.70727468C>G	GRCh38
NC_000014.8:g.71194185C>G , CM000676.1:g.71194185C>G	GRCh37
NC_000014.7:g.70263938C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000554752.7:c.*2912G>C MANE Select	ENSP00000451612.2:n.*2912G>C
ENST00000554752.6:c.6227G>C	ENSP00000451612.2:n.6227G>C
ENST00000611979.4:c.5555G>C	ENSP00000480011.1:n.5555G>C
NM_001284230.1:c.6227G>C	NP_001271159.1:n.6227G>C
NM_001284231.1:c.*2912G>C	NP_001271160.1:n.*2912G>C
NM_001284232.1:c.*2912G>C	NP_001271161.1:n.*2912G>C
NM_033141.3:c.6269G>C	NP_149132.2:n.6269G>C
XM_005267683.3:c.*2912G>C	XP_005267740.1:n.*2912G>C
XM_011536788.1:c.*2912G>C	XP_011535090.1:n.*2912G>C
XM_011536789.1:c.*2912G>C	XP_011535091.1:n.*2912G>C
XM_011536790.1:c.*2912G>C	XP_011535092.1:n.*2912G>C
XM_011536791.1:c.*2912G>C	XP_011535093.1:n.*2912G>C
XM_011536792.1:c.*2912G>C	XP_011535094.1:n.*2912G>C
XM_011536793.1:c.*2912G>C	XP_011535095.1:n.*2912G>C
XM_011536794.1:c.*2912G>C	XP_011535096.1:n.*2912G>C
XM_005267683.5:c.*2912G>C	XP_005267740.1:n.*2912G>C
XM_011536788.3:c.*2912G>C	XP_011535090.1:n.*2912G>C
XM_011536794.2:c.*2912G>C	XP_011535096.1:n.*2912G>C
NM_033141.4:c.*2912G>C	NP_149132.2:n.*2912G>C
NM_001284230.2:c.*2912G>C MANE Select	NP_001271159.1:n.*2912G>C