Canonical Allele Identifier: CA7624145

Gene: MAP2K1 SNAPC5

Linked Data

• dbSNP Id: rs756730939
• ExAC: 15:66782790 GTTTTT / G
• gnomAD v2: 15-66782790-GTTTTT-G
• gnomAD v4: 15-66490452-GTTTTT-G
• MyVariant Identifiers: chr15:g.66782791_66782795del (hg19) ; chr15:g.66490453_66490457del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66490455_66490459del , CM000677.2:g.66490455_66490459del	GRCh38
NC_000015.9:g.66782793_66782797del , CM000677.1:g.66782793_66782797del	GRCh37
NC_000015.8:g.64569847_64569851del	NCBI36
NG_008305.1:g.108583_108587del , LRG_725:g.108583_108587del
NG_051234.1:g.12359_12363del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.*117-47_*117-43del (MAP2K1)	ENSP00000508681.1:n.*117-47_*117-43del
ENST00000685172.1:c.1023-47_1023-43del (MAP2K1)	ENSP00000509604.1:n.1023-47_1023-43del
ENST00000685763.1:c.922-47_922-43del (MAP2K1)	ENSP00000509016.1:n.922-47_922-43del
ENST00000686347.1:c.742-47_742-43del (MAP2K1)	ENSP00000509027.1:n.742-47_742-43del
ENST00000687191.1:n.3349-47_3349-43del (MAP2K1)
ENST00000687481.1:n.484-47_484-43del (MAP2K1)
ENST00000688689.1:n.824-47_824-43del (MAP2K1)
ENST00000689951.1:c.1120-47_1120-43del (MAP2K1)	ENSP00000509308.1:n.1120-47_1120-43del
ENST00000691077.1:c.*2228-47_*2228-43del (MAP2K1)	ENSP00000509843.1:n.*2228-47_*2228-43del
ENST00000691576.1:c.940-47_940-43del (MAP2K1)	ENSP00000510066.1:n.940-47_940-43del
ENST00000691937.1:c.*50-47_*50-43del (MAP2K1)	ENSP00000508768.1:n.*50-47_*50-43del
ENST00000692487.1:c.*2669-47_*2669-43del (MAP2K1)	ENSP00000509534.1:n.*2669-47_*2669-43del
ENST00000692683.1:c.1003-47_1003-43del (MAP2K1)	ENSP00000508437.1:n.1003-47_1003-43del
ENST00000693150.1:c.925-47_925-43del (MAP2K1)	ENSP00000510309.1:n.925-47_925-43del
ENST00000307102.10:c.1069-47_1069-43del (MAP2K1) MANE Select	ENSP00000302486.5:n.1069-47_1069-43del
ENST00000307102.9:c.1069-47_1069-43del (MAP2K1)	ENSP00000302486.4:n.1069-47_1069-43del
ENST00000395589.6:c.*282_*286del (SNAPC5)	ENSP00000378954.2:n.*282_*286del
ENST00000563480.6:c.*282_*286del (SNAPC5)	ENSP00000457892.1:n.*282_*286del
ENST00000566326.1:c.541-47_541-43del (MAP2K1)	ENSP00000456438.1:n.541-47_541-43del
NM_002755.3:c.1069-47_1069-43del , LRG_725t1:c.1069-47_1069-43del (MAP2K1)	NP_002746.1:n.1069-47_1069-43del
NM_006049.2:c.*282_*286del (SNAPC5)	NP_006040.1:n.*282_*286del
XM_011521783.1:c.1003-47_1003-43del (MAP2K1)	XP_011520085.1:n.1003-47_1003-43del
NM_006049.3:c.*282_*286del (SNAPC5)	NP_006040.1:n.*282_*286del
NR_138061.1:n.801_805del (SNAPC5)
XM_011521783.3:c.1003-47_1003-43del (MAP2K1)	XP_011520085.1:n.1003-47_1003-43del
XM_017022411.2:c.991-47_991-43del (MAP2K1)	XP_016877900.1:n.991-47_991-43del
XM_017022412.1:c.925-47_925-43del (MAP2K1)	XP_016877901.1:n.925-47_925-43del
XM_017022413.1:c.541-47_541-43del (MAP2K1)	XP_016877902.1:n.541-47_541-43del
NM_002755.4:c.1069-47_1069-43del (MAP2K1) MANE Select	NP_002746.1:n.1069-47_1069-43del
NM_006049.4:c.*282_*286del (SNAPC5)	NP_006040.1:n.*282_*286del
NR_138061.2:n.748_752del (SNAPC5)