Canonical Allele Identifier: CA2625486065

Gene: MAP3K9

Linked Data

• gnomAD v4: 14-70727443-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.70727443A>C , CM000676.2:g.70727443A>C	GRCh38
NC_000014.8:g.71194160A>C , CM000676.1:g.71194160A>C	GRCh37
NC_000014.7:g.70263913A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000554752.7:c.*2937T>G MANE Select	ENSP00000451612.2:n.*2937T>G
ENST00000554752.6:c.6252T>G	ENSP00000451612.2:n.6252T>G
ENST00000611979.4:c.5580T>G	ENSP00000480011.1:n.5580T>G
NM_001284230.1:c.6252T>G	NP_001271159.1:n.6252T>G
NM_001284231.1:c.*2937T>G	NP_001271160.1:n.*2937T>G
NM_001284232.1:c.*2937T>G	NP_001271161.1:n.*2937T>G
NM_033141.3:c.6294T>G	NP_149132.2:n.6294T>G
XM_005267683.3:c.*2937T>G	XP_005267740.1:n.*2937T>G
XM_011536788.1:c.*2937T>G	XP_011535090.1:n.*2937T>G
XM_011536789.1:c.*2937T>G	XP_011535091.1:n.*2937T>G
XM_011536790.1:c.*2937T>G	XP_011535092.1:n.*2937T>G
XM_011536791.1:c.*2937T>G	XP_011535093.1:n.*2937T>G
XM_011536792.1:c.*2937T>G	XP_011535094.1:n.*2937T>G
XM_011536793.1:c.*2937T>G	XP_011535095.1:n.*2937T>G
XM_011536794.1:c.*2937T>G	XP_011535096.1:n.*2937T>G
XM_005267683.5:c.*2937T>G	XP_005267740.1:n.*2937T>G
XM_011536788.3:c.*2937T>G	XP_011535090.1:n.*2937T>G
XM_011536794.2:c.*2937T>G	XP_011535096.1:n.*2937T>G
NM_033141.4:c.*2937T>G	NP_149132.2:n.*2937T>G
NM_001284230.2:c.*2937T>G MANE Select	NP_001271159.1:n.*2937T>G