Canonical Allele Identifier: CA490861830

Gene: MAP2K1 SNAPC5

Linked Data

• MyVariant Identifiers: chr15:g.66782771T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66490433T>A , CM000677.2:g.66490433T>A	GRCh38
NC_000015.9:g.66782771T>A , CM000677.1:g.66782771T>A	GRCh37
NC_000015.8:g.64569825T>A	NCBI36
NG_008305.1:g.108561T>A , LRG_725:g.108561T>A
NG_051234.1:g.12383A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.*117-69T>A (MAP2K1)	ENSP00000508681.1:n.*117-69T>A
ENST00000685172.1:c.1023-69T>A (MAP2K1)	ENSP00000509604.1:n.1023-69T>A
ENST00000685763.1:c.922-69T>A (MAP2K1)	ENSP00000509016.1:n.922-69T>A
ENST00000686347.1:c.742-69T>A (MAP2K1)	ENSP00000509027.1:n.742-69T>A
ENST00000687191.1:n.3349-69T>A (MAP2K1)
ENST00000687481.1:n.484-69T>A (MAP2K1)
ENST00000688689.1:n.824-69T>A (MAP2K1)
ENST00000689951.1:c.1120-69T>A (MAP2K1)	ENSP00000509308.1:n.1120-69T>A
ENST00000691077.1:c.*2228-69T>A (MAP2K1)	ENSP00000509843.1:n.*2228-69T>A
ENST00000691576.1:c.940-69T>A (MAP2K1)	ENSP00000510066.1:n.940-69T>A
ENST00000691937.1:c.*50-69T>A (MAP2K1)	ENSP00000508768.1:n.*50-69T>A
ENST00000692487.1:c.*2669-69T>A (MAP2K1)	ENSP00000509534.1:n.*2669-69T>A
ENST00000692683.1:c.1003-69T>A (MAP2K1)	ENSP00000508437.1:n.1003-69T>A
ENST00000693150.1:c.925-69T>A (MAP2K1)	ENSP00000510309.1:n.925-69T>A
ENST00000307102.10:c.1069-69T>A (MAP2K1) MANE Select	ENSP00000302486.5:n.1069-69T>A
ENST00000307102.9:c.1069-69T>A (MAP2K1)	ENSP00000302486.4:n.1069-69T>A
ENST00000395589.6:c.*306A>T (SNAPC5)	ENSP00000378954.2:n.*306A>T
ENST00000563480.6:c.*306A>T (SNAPC5)	ENSP00000457892.1:n.*306A>T
ENST00000566326.1:c.541-69T>A (MAP2K1)	ENSP00000456438.1:n.541-69T>A
NM_002755.3:c.1069-69T>A , LRG_725t1:c.1069-69T>A (MAP2K1)	NP_002746.1:n.1069-69T>A
NM_006049.2:c.*306A>T (SNAPC5)	NP_006040.1:n.*306A>T
XM_011521783.1:c.1003-69T>A (MAP2K1)	XP_011520085.1:n.1003-69T>A
NM_006049.3:c.*306A>T (SNAPC5)	NP_006040.1:n.*306A>T
NR_138061.1:n.825A>T (SNAPC5)
XM_011521783.3:c.1003-69T>A (MAP2K1)	XP_011520085.1:n.1003-69T>A
XM_017022411.2:c.991-69T>A (MAP2K1)	XP_016877900.1:n.991-69T>A
XM_017022412.1:c.925-69T>A (MAP2K1)	XP_016877901.1:n.925-69T>A
XM_017022413.1:c.541-69T>A (MAP2K1)	XP_016877902.1:n.541-69T>A
NM_002755.4:c.1069-69T>A (MAP2K1) MANE Select	NP_002746.1:n.1069-69T>A
NM_006049.4:c.*306A>T (SNAPC5)	NP_006040.1:n.*306A>T
NR_138061.2:n.772A>T (SNAPC5)