Canonical Allele Identifier: CA14065531

Gene: MAP3K9

Linked Data

• dbSNP Id: rs17108533
• gnomAD v2: 14-71249802-C-T
• gnomAD v3: 14-70783085-C-T
• gnomAD v4: 14-70783085-C-T
• MyVariant Identifiers: chr14:g.71249802C>T (hg19) ; chr14:g.70783085C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.70783085C>T , CM000676.2:g.70783085C>T	GRCh38
NC_000014.8:g.71249802C>T , CM000676.1:g.71249802C>T	GRCh37
NC_000014.7:g.70319555C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000554752.7:c.820+17582G>A MANE Select	ENSP00000451612.2:n.820+17582G>A
ENST00000381250.8:c.820+17582G>A	ENSP00000370649.4:n.820+17582G>A
ENST00000553414.5:c.-99+138G>A	ENSP00000451038.1:n.-99+138G>A
ENST00000554146.1:c.-16+138G>A	ENSP00000451921.1:n.-16+138G>A
ENST00000554752.6:c.820+17582G>A	ENSP00000451612.2:n.820+17582G>A
ENST00000555993.6:c.820+17582G>A	ENSP00000451263.2:n.820+17582G>A
NM_001284230.1:c.820+17582G>A	NP_001271159.1:n.820+17582G>A
NM_001284231.1:c.-16+138G>A	NP_001271160.1:n.-16+138G>A
NM_001284232.1:c.-99+138G>A	NP_001271161.1:n.-99+138G>A
NM_033141.3:c.820+17582G>A	NP_149132.2:n.820+17582G>A
XM_005267683.3:c.820+17582G>A	XP_005267740.1:n.820+17582G>A
XM_011536788.1:c.820+17582G>A	XP_011535090.1:n.820+17582G>A
XM_011536789.1:c.820+17582G>A	XP_011535091.1:n.820+17582G>A
XM_011536790.1:c.820+17582G>A	XP_011535092.1:n.820+17582G>A
XM_011536791.1:c.820+17582G>A	XP_011535093.1:n.820+17582G>A
XM_011536792.1:c.-99+138G>A	XP_011535094.1:n.-99+138G>A
XM_005267683.5:c.820+17582G>A	XP_005267740.1:n.820+17582G>A
XM_011536788.3:c.820+17582G>A	XP_011535090.1:n.820+17582G>A
NM_033141.4:c.820+17582G>A	NP_149132.2:n.820+17582G>A
NM_001284230.2:c.820+17582G>A MANE Select	NP_001271159.1:n.820+17582G>A