Canonical Allele Identifier: CA2184089927
Gene: MAP2K1 HGNC NCBI
SNAPC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66490563C= , CM000677.2:g.66490563C= GRCh38
NC_000015.9:g.66782901C= , CM000677.1:g.66782901C= GRCh37
NC_000015.8:g.64569955C= NCBI36
NG_008305.1:g.108691C= , LRG_725:g.108691C=
NG_051234.1:g.12253G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.*178C= (MAP2K1) ENSP00000508681.1:n.*178C=
ENST00000685172.1:c.1084C= (MAP2K1) ENSP00000509604.1:p.Pro362=
ENST00000685763.1:c.983C= (MAP2K1) ENSP00000509016.1:p.Ser328=
ENST00000686347.1:c.803C= (MAP2K1) ENSP00000509027.1:p.Ser268=
ENST00000687191.1:n.3410C= (MAP2K1)
ENST00000687481.1:n.545C= (MAP2K1)
ENST00000688689.1:n.885C= (MAP2K1)
ENST00000689951.1:c.1181C= (MAP2K1) ENSP00000509308.1:p.Ser394=
ENST00000691077.1:c.*2289C= (MAP2K1) ENSP00000509843.1:n.*2289C=
ENST00000691576.1:c.1001C= (MAP2K1) ENSP00000510066.1:p.Ser334=
ENST00000691937.1:c.*111C= (MAP2K1) ENSP00000508768.1:n.*111C=
ENST00000692487.1:c.*2730C= (MAP2K1) ENSP00000509534.1:n.*2730C=
ENST00000692683.1:c.1064C= (MAP2K1) ENSP00000508437.1:p.Ser355=
ENST00000693150.1:c.986C= (MAP2K1) ENSP00000510309.1:p.Ser329=
ENST00000307102.10:c.1130C= (MAP2K1) MANE Select ENSP00000302486.5:p.Ser377=
ENST00000307102.9:c.1130C= (MAP2K1) ENSP00000302486.4:p.Ser377=
ENST00000395589.6:c.*176G= (SNAPC5) ENSP00000378954.2:n.*176G=
ENST00000563480.6:c.*176G= (SNAPC5) ENSP00000457892.1:n.*176G=
ENST00000566326.1:c.602C= (MAP2K1) ENSP00000456438.1:p.Ser201=
NM_002755.3:c.1130C= , LRG_725t1:c.1130C= (MAP2K1) NP_002746.1:p.Ser377=
NM_006049.2:c.*176G= (SNAPC5) NP_006040.1:n.*176G=
XM_011521783.1:c.1064C= (MAP2K1) XP_011520085.1:p.Ser355=
NM_006049.3:c.*176G= (SNAPC5) NP_006040.1:n.*176G=
NR_138061.1:n.695G= (SNAPC5)
XM_011521783.3:c.1064C= (MAP2K1) XP_011520085.1:p.Ser355=
XM_017022411.2:c.1052C= (MAP2K1) XP_016877900.1:p.Ser351=
XM_017022412.1:c.986C= (MAP2K1) XP_016877901.1:p.Ser329=
XM_017022413.1:c.602C= (MAP2K1) XP_016877902.1:p.Ser201=
NM_002755.4:c.1130C= (MAP2K1) MANE Select NP_002746.1:p.Ser377=
NM_006049.4:c.*176G= (SNAPC5) NP_006040.1:n.*176G=
NR_138061.2:n.642G= (SNAPC5)