Canonical Allele Identifier: CA2629083378

Gene: MAP2K1

Linked Data

• gnomAD v4: 15-66481694-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66481694C>T , CM000677.2:g.66481694C>T	GRCh38
NC_000015.9:g.66774032C>T , CM000677.1:g.66774032C>T	GRCh37
NC_000015.8:g.64561086C>T	NCBI36
NG_008305.1:g.99822C>T , LRG_725:g.99822C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.503-61C>T	ENSP00000508681.1:n.503-61C>T
ENST00000685172.1:c.569-61C>T	ENSP00000509604.1:n.569-61C>T
ENST00000685763.1:c.422-61C>T	ENSP00000509016.1:n.422-61C>T
ENST00000686347.1:c.569-5534C>T	ENSP00000509027.1:n.569-5534C>T
ENST00000687191.1:n.927-61C>T
ENST00000689951.1:c.620-61C>T	ENSP00000509308.1:n.620-61C>T
ENST00000691077.1:c.569-61C>T	ENSP00000509843.1:n.569-61C>T
ENST00000691576.1:c.569-3300C>T	ENSP00000510066.1:n.569-3300C>T
ENST00000691937.1:c.569-61C>T	ENSP00000508768.1:n.569-61C>T
ENST00000692487.1:c.569-61C>T	ENSP00000509534.1:n.569-61C>T
ENST00000692683.1:c.503-61C>T	ENSP00000508437.1:n.503-61C>T
ENST00000693150.1:c.425-61C>T	ENSP00000510309.1:n.425-61C>T
ENST00000307102.10:c.569-61C>T MANE Select	ENSP00000302486.5:n.569-61C>T
ENST00000307102.9:c.569-61C>T	ENSP00000302486.4:n.569-61C>T
ENST00000566326.1:c.41-61C>T	ENSP00000456438.1:n.41-61C>T
NM_002755.3:c.569-61C>T , LRG_725t1:c.569-61C>T	NP_002746.1:n.569-61C>T
XM_011521783.1:c.503-61C>T	XP_011520085.1:n.503-61C>T
XM_011521783.3:c.503-61C>T	XP_011520085.1:n.503-61C>T
XM_017022411.2:c.491-61C>T	XP_016877900.1:n.491-61C>T
XM_017022412.1:c.425-61C>T	XP_016877901.1:n.425-61C>T
XM_017022413.1:c.41-61C>T	XP_016877902.1:n.41-61C>T
NM_002755.4:c.569-61C>T MANE Select	NP_002746.1:n.569-61C>T