Canonical Allele Identifier: CA1548115934
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56832039G= , CM000667.2:g.56832039G= GRCh38
NC_000005.9:g.56127866G= , CM000667.1:g.56127866G= GRCh37
NC_000005.8:g.56163623G= NCBI36
NG_031884.1:g.21967G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.482+15984G= MANE Select ENSP00000382423.3:n.482+15984G=
ENST00000399503.3:c.482+15984G= ENSP00000382423.3:n.482+15984G=
NM_005921.1:c.482+15984G= NP_005912.1:n.482+15984G=
XM_005248519.3:c.104+11223G= XP_005248576.2:n.104+11223G=
XM_011543406.1:c.227+15704G= XP_011541708.1:n.227+15704G=
XM_011543407.1:c.482+15984G= XP_011541709.1:n.482+15984G=
XM_011543408.1:c.482+15984G= XP_011541710.1:n.482+15984G=
XM_017009484.1:c.71+11223G= XP_016864973.1:n.71+11223G=
XM_017009485.1:c.-8+14923G= XP_016864974.1:n.-8+14923G=
XR_001742068.2:n.513+15984G=
NM_005921.2:c.482+15984G= MANE Select NP_005912.1:n.482+15984G=