Canonical Allele Identifier: CA13991628
Gene: MAP4K5 HGNC NCBI

Linked Data

dbSNP Id: rs17718580

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50506914C>T , CM000676.2:g.50506914C>T GRCh38
NC_000014.8:g.50973632C>T , CM000676.1:g.50973632C>T GRCh37
NC_000014.7:g.50043382C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000013125.9:c.109-2057G>A ENSP00000013125.5:n.109-2057G>A
ENST00000557390.6:c.109-2057G>A ENSP00000451980.2:n.109-2057G>A
ENST00000682126.1:c.109-2057G>A MANE Select ENSP00000507200.1:n.109-2057G>A
ENST00000013125.8:c.109-2057G>A ENSP00000013125.4:n.109-2057G>A
ENST00000554091.5:c.109-2057G>A ENSP00000451926.1:n.109-2057G>A
ENST00000554273.1:c.109-2057G>A ENSP00000451452.1:n.109-2057G>A
ENST00000555216.5:c.-93-2057G>A ENSP00000452289.1:n.-93-2057G>A
ENST00000557390.5:c.109-2057G>A ENSP00000451980.1:n.109-2057G>A
NM_006575.4:c.109-2057G>A NP_006566.2:n.109-2057G>A
NM_198794.2:c.109-2057G>A NP_942089.1:n.109-2057G>A
XM_006720013.2:c.109-2057G>A XP_006720076.1:n.109-2057G>A
XM_011536377.1:c.109-2057G>A XP_011534679.1:n.109-2057G>A
XM_011536378.1:c.-93-2057G>A XP_011534680.1:n.-93-2057G>A
XM_006720013.4:c.109-2057G>A XP_006720076.1:n.109-2057G>A
XM_011536377.3:c.109-2057G>A XP_011534679.1:n.109-2057G>A
XM_011536378.3:c.-93-2057G>A XP_011534680.1:n.-93-2057G>A
XM_024449461.1:c.109-2057G>A XP_024305229.1:n.109-2057G>A
NM_006575.5:c.109-2057G>A NP_006566.2:n.109-2057G>A
NM_198794.3:c.109-2057G>A NP_942089.1:n.109-2057G>A
NM_006575.6:c.109-2057G>A MANE Select NP_006566.2:n.109-2057G>A
NM_198794.4:c.109-2057G>A NP_942089.1:n.109-2057G>A