Canonical Allele Identifier: CA1548129277
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859934A= , CM000667.2:g.56859934A= GRCh38
NC_000005.9:g.56155761A= , CM000667.1:g.56155761A= GRCh37
NC_000005.8:g.56191518A= NCBI36
NG_031884.1:g.49862A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.834+19A= MANE Select ENSP00000382423.3:n.834+19A=
ENST00000399503.3:c.834+19A= ENSP00000382423.3:n.834+19A=
NM_005921.1:c.834+19A= NP_005912.1:n.834+19A=
XM_005248519.3:c.456+19A= XP_005248576.2:n.456+19A=
XM_011543406.1:c.579+19A= XP_011541708.1:n.579+19A=
XM_011543407.1:c.834+19A= XP_011541709.1:n.834+19A=
XM_011543408.1:c.834+19A= XP_011541710.1:n.834+19A=
XM_017009484.1:c.423+19A= XP_016864973.1:n.423+19A=
XM_017009485.1:c.345+19A= XP_016864974.1:n.345+19A=
XR_001742068.2:n.865+19A=
NM_005921.2:c.834+19A= MANE Select NP_005912.1:n.834+19A=