Canonical Allele Identifier: CA490861948

Gene: MAP2K1 SNAPC5

Linked Data

• MyVariant Identifiers: chr15:g.66782814A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66490476A>G , CM000677.2:g.66490476A>G	GRCh38
NC_000015.9:g.66782814A>G , CM000677.1:g.66782814A>G	GRCh37
NC_000015.8:g.64569868A>G	NCBI36
NG_008305.1:g.108604A>G , LRG_725:g.108604A>G
NG_051234.1:g.12340T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.*117-26A>G (MAP2K1)	ENSP00000508681.1:n.*117-26A>G
ENST00000685172.1:c.1023-26A>G (MAP2K1)	ENSP00000509604.1:n.1023-26A>G
ENST00000685763.1:c.922-26A>G (MAP2K1)	ENSP00000509016.1:n.922-26A>G
ENST00000686347.1:c.742-26A>G (MAP2K1)	ENSP00000509027.1:n.742-26A>G
ENST00000687191.1:n.3349-26A>G (MAP2K1)
ENST00000687481.1:n.484-26A>G (MAP2K1)
ENST00000688689.1:n.824-26A>G (MAP2K1)
ENST00000689951.1:c.1120-26A>G (MAP2K1)	ENSP00000509308.1:n.1120-26A>G
ENST00000691077.1:c.*2228-26A>G (MAP2K1)	ENSP00000509843.1:n.*2228-26A>G
ENST00000691576.1:c.940-26A>G (MAP2K1)	ENSP00000510066.1:n.940-26A>G
ENST00000691937.1:c.*50-26A>G (MAP2K1)	ENSP00000508768.1:n.*50-26A>G
ENST00000692487.1:c.*2669-26A>G (MAP2K1)	ENSP00000509534.1:n.*2669-26A>G
ENST00000692683.1:c.1003-26A>G (MAP2K1)	ENSP00000508437.1:n.1003-26A>G
ENST00000693150.1:c.925-26A>G (MAP2K1)	ENSP00000510309.1:n.925-26A>G
ENST00000307102.10:c.1069-26A>G (MAP2K1) MANE Select	ENSP00000302486.5:n.1069-26A>G
ENST00000307102.9:c.1069-26A>G (MAP2K1)	ENSP00000302486.4:n.1069-26A>G
ENST00000395589.6:c.*263T>C (SNAPC5)	ENSP00000378954.2:n.*263T>C
ENST00000563480.6:c.*263T>C (SNAPC5)	ENSP00000457892.1:n.*263T>C
ENST00000566326.1:c.541-26A>G (MAP2K1)	ENSP00000456438.1:n.541-26A>G
NM_002755.3:c.1069-26A>G , LRG_725t1:c.1069-26A>G (MAP2K1)	NP_002746.1:n.1069-26A>G
NM_006049.2:c.*263T>C (SNAPC5)	NP_006040.1:n.*263T>C
XM_011521783.1:c.1003-26A>G (MAP2K1)	XP_011520085.1:n.1003-26A>G
NM_006049.3:c.*263T>C (SNAPC5)	NP_006040.1:n.*263T>C
NR_138061.1:n.782T>C (SNAPC5)
XM_011521783.3:c.1003-26A>G (MAP2K1)	XP_011520085.1:n.1003-26A>G
XM_017022411.2:c.991-26A>G (MAP2K1)	XP_016877900.1:n.991-26A>G
XM_017022412.1:c.925-26A>G (MAP2K1)	XP_016877901.1:n.925-26A>G
XM_017022413.1:c.541-26A>G (MAP2K1)	XP_016877902.1:n.541-26A>G
NM_002755.4:c.1069-26A>G (MAP2K1) MANE Select	NP_002746.1:n.1069-26A>G
NM_006049.4:c.*263T>C (SNAPC5)	NP_006040.1:n.*263T>C
NR_138061.2:n.729T>C (SNAPC5)