Canonical Allele Identifier: CA1548129231
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859835_56859838delinsTCTC , CM000667.2:g.56859835_56859838delinsTCTC GRCh38
NC_000005.9:g.56155662_56155665delinsTCTC , CM000667.1:g.56155662_56155665delinsTCTC GRCh37
NC_000005.8:g.56191419_56191422delinsTCTC NCBI36
NG_031884.1:g.49763_49766delinsTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.754_757delinsTCTC MANE Select ENSP00000382423.3:p.Ser252=
ENST00000399503.3:c.754_757delinsTCTC ENSP00000382423.3:p.Ser252=
NM_005921.1:c.754_757delinsTCTC NP_005912.1:p.Ser252=
XM_005248519.3:c.376_379delinsTCTC XP_005248576.2:p.Ser126=
XM_011543406.1:c.499_502delinsTCTC XP_011541708.1:p.Ser167=
XM_011543407.1:c.754_757delinsTCTC XP_011541709.1:p.Ser252=
XM_011543408.1:c.754_757delinsTCTC XP_011541710.1:p.Ser252=
XM_017009484.1:c.343_346delinsTCTC XP_016864973.1:p.Ser115=
XM_017009485.1:c.265_268delinsTCTC XP_016864974.1:p.Ser89=
XR_001742068.2:n.785_788delinsTCTC
NM_005921.2:c.754_757delinsTCTC MANE Select NP_005912.1:p.Ser252=