Canonical Allele Identifier: CA359802663
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs1416454518
gnomAD v3: 5-56859889-A-G
gnomAD v4: 5-56859889-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859889A>G , CM000667.2:g.56859889A>G GRCh38
NC_000005.9:g.56155716A>G , CM000667.1:g.56155716A>G GRCh37
NC_000005.8:g.56191473A>G NCBI36
NG_031884.1:g.49817A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.808A>G MANE Select ENSP00000382423.3:p.Arg270Gly
ENST00000399503.3:c.808A>G ENSP00000382423.3:p.Arg270Gly
NM_005921.1:c.808A>G NP_005912.1:p.Arg270Gly
XM_005248519.3:c.430A>G XP_005248576.2:p.Arg144Gly
XM_011543406.1:c.553A>G XP_011541708.1:p.Arg185Gly
XM_011543407.1:c.808A>G XP_011541709.1:p.Arg270Gly
XM_011543408.1:c.808A>G XP_011541710.1:p.Arg270Gly
XM_017009484.1:c.397A>G XP_016864973.1:p.Arg133Gly
XM_017009485.1:c.319A>G XP_016864974.1:p.Arg107Gly
XR_001742068.2:n.839A>G
NM_005921.2:c.808A>G MANE Select NP_005912.1:p.Arg270Gly