Canonical Allele Identifier: CA2673909960
Gene: MAP3K1 HGNC NCBI

Linked Data

gnomAD v4: 5-56881539-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881539T>G , CM000667.2:g.56881539T>G GRCh38
NC_000005.9:g.56177366T>G , CM000667.1:g.56177366T>G GRCh37
NC_000005.8:g.56213123T>G NCBI36
NG_031884.1:g.71467T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.2370-31T>G MANE Select ENSP00000382423.3:n.2370-31T>G
ENST00000399503.3:c.2370-31T>G ENSP00000382423.3:n.2370-31T>G
NM_005921.1:c.2370-31T>G NP_005912.1:n.2370-31T>G
XM_005248519.3:c.1992-31T>G XP_005248576.2:n.1992-31T>G
XM_011543406.1:c.2115-31T>G XP_011541708.1:n.2115-31T>G
XM_011543407.1:c.2091-31T>G XP_011541709.1:n.2091-31T>G
XM_011543408.1:c.2370-31T>G XP_011541710.1:n.2370-31T>G
XM_017009484.1:c.1959-31T>G XP_016864973.1:n.1959-31T>G
XM_017009485.1:c.1881-31T>G XP_016864974.1:n.1881-31T>G
XR_001742068.2:n.2401-31T>G
NM_005921.2:c.2370-31T>G MANE Select NP_005912.1:n.2370-31T>G