Canonical Allele Identifier: CA1548129217
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859809C= , CM000667.2:g.56859809C= GRCh38
NC_000005.9:g.56155636C= , CM000667.1:g.56155636C= GRCh37
NC_000005.8:g.56191393C= NCBI36
NG_031884.1:g.49737C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.728C= MANE Select ENSP00000382423.3:p.Pro243=
ENST00000399503.3:c.728C= ENSP00000382423.3:p.Pro243=
NM_005921.1:c.728C= NP_005912.1:p.Pro243=
XM_005248519.3:c.350C= XP_005248576.2:p.Pro117=
XM_011543406.1:c.473C= XP_011541708.1:p.Pro158=
XM_011543407.1:c.728C= XP_011541709.1:p.Pro243=
XM_011543408.1:c.728C= XP_011541710.1:p.Pro243=
XM_017009484.1:c.317C= XP_016864973.1:p.Pro106=
XM_017009485.1:c.239C= XP_016864974.1:p.Pro80=
XR_001742068.2:n.759C=
NM_005921.2:c.728C= MANE Select NP_005912.1:p.Pro243=