Canonical Allele Identifier: CA490861858

Gene: MAP2K1 SNAPC5

Linked Data

• MyVariant Identifiers: chr15:g.66782781G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66490443G>T , CM000677.2:g.66490443G>T	GRCh38
NC_000015.9:g.66782781G>T , CM000677.1:g.66782781G>T	GRCh37
NC_000015.8:g.64569835G>T	NCBI36
NG_008305.1:g.108571G>T , LRG_725:g.108571G>T
NG_051234.1:g.12373C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.*117-59G>T (MAP2K1)	ENSP00000508681.1:n.*117-59G>T
ENST00000685172.1:c.1023-59G>T (MAP2K1)	ENSP00000509604.1:n.1023-59G>T
ENST00000685763.1:c.922-59G>T (MAP2K1)	ENSP00000509016.1:n.922-59G>T
ENST00000686347.1:c.742-59G>T (MAP2K1)	ENSP00000509027.1:n.742-59G>T
ENST00000687191.1:n.3349-59G>T (MAP2K1)
ENST00000687481.1:n.484-59G>T (MAP2K1)
ENST00000688689.1:n.824-59G>T (MAP2K1)
ENST00000689951.1:c.1120-59G>T (MAP2K1)	ENSP00000509308.1:n.1120-59G>T
ENST00000691077.1:c.*2228-59G>T (MAP2K1)	ENSP00000509843.1:n.*2228-59G>T
ENST00000691576.1:c.940-59G>T (MAP2K1)	ENSP00000510066.1:n.940-59G>T
ENST00000691937.1:c.*50-59G>T (MAP2K1)	ENSP00000508768.1:n.*50-59G>T
ENST00000692487.1:c.*2669-59G>T (MAP2K1)	ENSP00000509534.1:n.*2669-59G>T
ENST00000692683.1:c.1003-59G>T (MAP2K1)	ENSP00000508437.1:n.1003-59G>T
ENST00000693150.1:c.925-59G>T (MAP2K1)	ENSP00000510309.1:n.925-59G>T
ENST00000307102.10:c.1069-59G>T (MAP2K1) MANE Select	ENSP00000302486.5:n.1069-59G>T
ENST00000307102.9:c.1069-59G>T (MAP2K1)	ENSP00000302486.4:n.1069-59G>T
ENST00000395589.6:c.*296C>A (SNAPC5)	ENSP00000378954.2:n.*296C>A
ENST00000563480.6:c.*296C>A (SNAPC5)	ENSP00000457892.1:n.*296C>A
ENST00000566326.1:c.541-59G>T (MAP2K1)	ENSP00000456438.1:n.541-59G>T
NM_002755.3:c.1069-59G>T , LRG_725t1:c.1069-59G>T (MAP2K1)	NP_002746.1:n.1069-59G>T
NM_006049.2:c.*296C>A (SNAPC5)	NP_006040.1:n.*296C>A
XM_011521783.1:c.1003-59G>T (MAP2K1)	XP_011520085.1:n.1003-59G>T
NM_006049.3:c.*296C>A (SNAPC5)	NP_006040.1:n.*296C>A
NR_138061.1:n.815C>A (SNAPC5)
XM_011521783.3:c.1003-59G>T (MAP2K1)	XP_011520085.1:n.1003-59G>T
XM_017022411.2:c.991-59G>T (MAP2K1)	XP_016877900.1:n.991-59G>T
XM_017022412.1:c.925-59G>T (MAP2K1)	XP_016877901.1:n.925-59G>T
XM_017022413.1:c.541-59G>T (MAP2K1)	XP_016877902.1:n.541-59G>T
NM_002755.4:c.1069-59G>T (MAP2K1) MANE Select	NP_002746.1:n.1069-59G>T
NM_006049.4:c.*296C>A (SNAPC5)	NP_006040.1:n.*296C>A
NR_138061.2:n.762C>A (SNAPC5)