Canonical Allele Identifier: CA392939043

Gene: MAP2K1 SNAPC5

Linked Data

• MyVariant Identifiers: chr15:g.66782901C>G (hg19) ; chr15:g.66490563C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.*178C>G (MAP2K1)	ENSP00000508681.1:n.*178C>G
ENST00000685172.1:c.1084C>G (MAP2K1)	ENSP00000509604.1:p.Pro362Ala
ENST00000685763.1:c.983C>G (MAP2K1)	ENSP00000509016.1:p.Ser328Cys
ENST00000686347.1:c.803C>G (MAP2K1)	ENSP00000509027.1:p.Ser268Cys
ENST00000687191.1:n.3410C>G (MAP2K1)
ENST00000687481.1:n.545C>G (MAP2K1)
ENST00000688689.1:n.885C>G (MAP2K1)
ENST00000689951.1:c.1181C>G (MAP2K1)	ENSP00000509308.1:p.Ser394Cys
ENST00000691077.1:c.*2289C>G (MAP2K1)	ENSP00000509843.1:n.*2289C>G
ENST00000691576.1:c.1001C>G (MAP2K1)	ENSP00000510066.1:p.Ser334Cys
ENST00000691937.1:c.*111C>G (MAP2K1)	ENSP00000508768.1:n.*111C>G
ENST00000692487.1:c.*2730C>G (MAP2K1)	ENSP00000509534.1:n.*2730C>G
ENST00000692683.1:c.1064C>G (MAP2K1)	ENSP00000508437.1:p.Ser355Cys
ENST00000693150.1:c.986C>G (MAP2K1)	ENSP00000510309.1:p.Ser329Cys
ENST00000307102.10:c.1130C>G (MAP2K1) MANE Select	ENSP00000302486.5:p.Ser377Cys
ENST00000307102.9:c.1130C>G (MAP2K1)	ENSP00000302486.4:p.Ser377Cys
ENST00000395589.6:c.*176G>C (SNAPC5)	ENSP00000378954.2:n.*176G>C
ENST00000563480.6:c.*176G>C (SNAPC5)	ENSP00000457892.1:n.*176G>C
ENST00000566326.1:c.602C>G (MAP2K1)	ENSP00000456438.1:p.Ser201Cys
NM_002755.3:c.1130C>G , LRG_725t1:c.1130C>G (MAP2K1)	NP_002746.1:p.Ser377Cys
NM_006049.2:c.*176G>C (SNAPC5)	NP_006040.1:n.*176G>C
XM_011521783.1:c.1064C>G (MAP2K1)	XP_011520085.1:p.Ser355Cys
NM_006049.3:c.*176G>C (SNAPC5)	NP_006040.1:n.*176G>C
NR_138061.1:n.695G>C (SNAPC5)
XM_011521783.3:c.1064C>G (MAP2K1)	XP_011520085.1:p.Ser355Cys
XM_017022411.2:c.1052C>G (MAP2K1)	XP_016877900.1:p.Ser351Cys
XM_017022412.1:c.986C>G (MAP2K1)	XP_016877901.1:p.Ser329Cys
XM_017022413.1:c.602C>G (MAP2K1)	XP_016877902.1:p.Ser201Cys
NM_002755.4:c.1130C>G (MAP2K1) MANE Select	NP_002746.1:p.Ser377Cys
NM_006049.4:c.*176G>C (SNAPC5)	NP_006040.1:n.*176G>C
NR_138061.2:n.642G>C (SNAPC5)