Canonical Allele Identifier: CA392938914

Gene: MAP2K1 SNAPC5

Linked Data

• MyVariant Identifiers: chr15:g.66782873G>C (hg19) ; chr15:g.66490535G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66490535G>C , CM000677.2:g.66490535G>C	GRCh38
NC_000015.9:g.66782873G>C , CM000677.1:g.66782873G>C	GRCh37
NC_000015.8:g.64569927G>C	NCBI36
NG_008305.1:g.108663G>C , LRG_725:g.108663G>C
NG_051234.1:g.12281C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.*150G>C (MAP2K1)	ENSP00000508681.1:n.*150G>C
ENST00000685172.1:c.1056G>C (MAP2K1)	ENSP00000509604.1:p.Arg352Ser
ENST00000685763.1:c.955G>C (MAP2K1)	ENSP00000509016.1:p.Glu319Gln
ENST00000686347.1:c.775G>C (MAP2K1)	ENSP00000509027.1:p.Glu259Gln
ENST00000687191.1:n.3382G>C (MAP2K1)
ENST00000687481.1:n.517G>C (MAP2K1)
ENST00000688689.1:n.857G>C (MAP2K1)
ENST00000689951.1:c.1153G>C (MAP2K1)	ENSP00000509308.1:p.Glu385Gln
ENST00000691077.1:c.*2261G>C (MAP2K1)	ENSP00000509843.1:n.*2261G>C
ENST00000691576.1:c.973G>C (MAP2K1)	ENSP00000510066.1:p.Glu325Gln
ENST00000691937.1:c.*83G>C (MAP2K1)	ENSP00000508768.1:n.*83G>C
ENST00000692487.1:c.*2702G>C (MAP2K1)	ENSP00000509534.1:n.*2702G>C
ENST00000692683.1:c.1036G>C (MAP2K1)	ENSP00000508437.1:p.Glu346Gln
ENST00000693150.1:c.958G>C (MAP2K1)	ENSP00000510309.1:p.Glu320Gln
ENST00000307102.10:c.1102G>C (MAP2K1) MANE Select	ENSP00000302486.5:p.Glu368Gln
ENST00000307102.9:c.1102G>C (MAP2K1)	ENSP00000302486.4:p.Glu368Gln
ENST00000395589.6:c.*204C>G (SNAPC5)	ENSP00000378954.2:n.*204C>G
ENST00000563480.6:c.*204C>G (SNAPC5)	ENSP00000457892.1:n.*204C>G
ENST00000566326.1:c.574G>C (MAP2K1)	ENSP00000456438.1:p.Glu192Gln
NM_002755.3:c.1102G>C , LRG_725t1:c.1102G>C (MAP2K1)	NP_002746.1:p.Glu368Gln
NM_006049.2:c.*204C>G (SNAPC5)	NP_006040.1:n.*204C>G
XM_011521783.1:c.1036G>C (MAP2K1)	XP_011520085.1:p.Glu346Gln
NM_006049.3:c.*204C>G (SNAPC5)	NP_006040.1:n.*204C>G
NR_138061.1:n.723C>G (SNAPC5)
XM_011521783.3:c.1036G>C (MAP2K1)	XP_011520085.1:p.Glu346Gln
XM_017022411.2:c.1024G>C (MAP2K1)	XP_016877900.1:p.Glu342Gln
XM_017022412.1:c.958G>C (MAP2K1)	XP_016877901.1:p.Glu320Gln
XM_017022413.1:c.574G>C (MAP2K1)	XP_016877902.1:p.Glu192Gln
NM_002755.4:c.1102G>C (MAP2K1) MANE Select	NP_002746.1:p.Glu368Gln
NM_006049.4:c.*204C>G (SNAPC5)	NP_006040.1:n.*204C>G
NR_138061.2:n.670C>G (SNAPC5)