Canonical Allele Identifier: CA11578610

Gene: MAP3K13

Linked Data

• dbSNP Id: rs7629245
• gnomAD v2: 3-185141857-C-T
• gnomAD v3: 3-185424069-C-T
• gnomAD v4: 3-185424069-C-T
• MyVariant Identifiers: chr3:g.185141857C>T (hg19) ; chr3:g.185424069C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185424069C>T , CM000665.2:g.185424069C>T	GRCh38
NC_000003.11:g.185141857C>T , CM000665.1:g.185141857C>T	GRCh37
NC_000003.10:g.186624551C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265026.8:c.-85-4428C>T MANE Select	ENSP00000265026.3:n.-85-4428C>T
ENST00000265026.7:c.-85-4428C>T	ENSP00000265026.3:n.-85-4428C>T
ENST00000424227.5:c.-85-4428C>T	ENSP00000399910.1:n.-85-4428C>T
ENST00000428617.1:c.-85-4428C>T	ENSP00000405163.1:n.-85-4428C>T
ENST00000433092.5:c.-85-4428C>T	ENSP00000389798.1:n.-85-4428C>T
ENST00000438053.5:c.-85-4428C>T	ENSP00000403561.1:n.-85-4428C>T
ENST00000443863.5:c.44-13378C>T	ENSP00000409325.1:n.44-13378C>T
ENST00000446828.5:c.39-19376C>T	ENSP00000411483.1:n.39-19376C>T
ENST00000447637.1:c.-85-4428C>T	ENSP00000389495.1:n.-85-4428C>T
NM_001242314.1:c.-85-4428C>T	NP_001229243.1:n.-85-4428C>T
NM_001242317.1:c.39-19376C>T	NP_001229246.1:n.39-19376C>T
NM_004721.4:c.-85-4428C>T	NP_004712.1:n.-85-4428C>T
XM_011513310.1:c.-85-4428C>T	XP_011511612.1:n.-85-4428C>T
XM_011513310.2:c.-85-4428C>T	XP_011511612.1:n.-85-4428C>T
XM_017007456.1:c.-85-4428C>T	XP_016862945.1:n.-85-4428C>T
XM_017007457.1:c.29-13378C>T	XP_016862946.1:n.29-13378C>T
XM_017007458.1:c.-671-4428C>T	XP_016862947.1:n.-671-4428C>T
XM_017007459.2:c.-671-4428C>T	XP_016862948.1:n.-671-4428C>T
NM_004721.5:c.-85-4428C>T MANE Select	NP_004712.1:n.-85-4428C>T
NM_001242314.2:c.-85-4428C>T	NP_001229243.1:n.-85-4428C>T
NM_001242317.2:c.39-19376C>T	NP_001229246.1:n.39-19376C>T