Canonical Allele Identifier: CA392939035

Gene: MAP2K1 SNAPC5

Linked Data

• MyVariant Identifiers: chr15:g.66782900T>A (hg19) ; chr15:g.66490562T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66490562T>A , CM000677.2:g.66490562T>A	GRCh38
NC_000015.9:g.66782900T>A , CM000677.1:g.66782900T>A	GRCh37
NC_000015.8:g.64569954T>A	NCBI36
NG_008305.1:g.108690T>A , LRG_725:g.108690T>A
NG_051234.1:g.12254A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.*177T>A (MAP2K1)	ENSP00000508681.1:n.*177T>A
ENST00000685172.1:c.1083T>A (MAP2K1)	ENSP00000509604.1:p.Ala361=
ENST00000685763.1:c.982T>A (MAP2K1)	ENSP00000509016.1:p.Ser328Thr
ENST00000686347.1:c.802T>A (MAP2K1)	ENSP00000509027.1:p.Ser268Thr
ENST00000687191.1:n.3409T>A (MAP2K1)
ENST00000687481.1:n.544T>A (MAP2K1)
ENST00000688689.1:n.884T>A (MAP2K1)
ENST00000689951.1:c.1180T>A (MAP2K1)	ENSP00000509308.1:p.Ser394Thr
ENST00000691077.1:c.*2288T>A (MAP2K1)	ENSP00000509843.1:n.*2288T>A
ENST00000691576.1:c.1000T>A (MAP2K1)	ENSP00000510066.1:p.Ser334Thr
ENST00000691937.1:c.*110T>A (MAP2K1)	ENSP00000508768.1:n.*110T>A
ENST00000692487.1:c.*2729T>A (MAP2K1)	ENSP00000509534.1:n.*2729T>A
ENST00000692683.1:c.1063T>A (MAP2K1)	ENSP00000508437.1:p.Ser355Thr
ENST00000693150.1:c.985T>A (MAP2K1)	ENSP00000510309.1:p.Ser329Thr
ENST00000307102.10:c.1129T>A (MAP2K1) MANE Select	ENSP00000302486.5:p.Ser377Thr
ENST00000307102.9:c.1129T>A (MAP2K1)	ENSP00000302486.4:p.Ser377Thr
ENST00000395589.6:c.*177A>T (SNAPC5)	ENSP00000378954.2:n.*177A>T
ENST00000563480.6:c.*177A>T (SNAPC5)	ENSP00000457892.1:n.*177A>T
ENST00000566326.1:c.601T>A (MAP2K1)	ENSP00000456438.1:p.Ser201Thr
NM_002755.3:c.1129T>A , LRG_725t1:c.1129T>A (MAP2K1)	NP_002746.1:p.Ser377Thr
NM_006049.2:c.*177A>T (SNAPC5)	NP_006040.1:n.*177A>T
XM_011521783.1:c.1063T>A (MAP2K1)	XP_011520085.1:p.Ser355Thr
NM_006049.3:c.*177A>T (SNAPC5)	NP_006040.1:n.*177A>T
NR_138061.1:n.696A>T (SNAPC5)
XM_011521783.3:c.1063T>A (MAP2K1)	XP_011520085.1:p.Ser355Thr
XM_017022411.2:c.1051T>A (MAP2K1)	XP_016877900.1:p.Ser351Thr
XM_017022412.1:c.985T>A (MAP2K1)	XP_016877901.1:p.Ser329Thr
XM_017022413.1:c.601T>A (MAP2K1)	XP_016877902.1:p.Ser201Thr
NM_002755.4:c.1129T>A (MAP2K1) MANE Select	NP_002746.1:p.Ser377Thr
NM_006049.4:c.*177A>T (SNAPC5)	NP_006040.1:n.*177A>T
NR_138061.2:n.643A>T (SNAPC5)