Canonical Allele Identifier: CA392936041

Gene: MAP2K1

Linked Data

• MyVariant Identifiers: chr15:g.66774093A>C (hg19) ; chr15:g.66481755A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66481755A>C , CM000677.2:g.66481755A>C	GRCh38
NC_000015.9:g.66774093A>C , CM000677.1:g.66774093A>C	GRCh37
NC_000015.8:g.64561147A>C	NCBI36
NG_008305.1:g.99883A>C , LRG_725:g.99883A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684779.1:c.503A>C	ENSP00000508681.1:p.Asp168Ala
ENST00000685172.1:c.569A>C	ENSP00000509604.1:p.Asp190Ala
ENST00000685763.1:c.422A>C	ENSP00000509016.1:p.Asp141Ala
ENST00000686347.1:c.569-5473A>C	ENSP00000509027.1:n.569-5473A>C
ENST00000687191.1:n.927A>C
ENST00000689951.1:c.620A>C	ENSP00000509308.1:p.Asn207Thr
ENST00000691077.1:c.569A>C	ENSP00000509843.1:p.Asp190Ala
ENST00000691576.1:c.569-3239A>C	ENSP00000510066.1:n.569-3239A>C
ENST00000691937.1:c.569A>C	ENSP00000508768.1:p.Asp190Ala
ENST00000692487.1:c.569A>C	ENSP00000509534.1:p.Asp190Ala
ENST00000692683.1:c.503A>C	ENSP00000508437.1:p.Asp168Ala
ENST00000693150.1:c.425A>C	ENSP00000510309.1:p.Asp142Ala
ENST00000307102.10:c.569A>C MANE Select	ENSP00000302486.5:p.Asp190Ala
ENST00000307102.9:c.569A>C	ENSP00000302486.4:p.Asp190Ala
ENST00000566326.1:c.41A>C	ENSP00000456438.1:p.Asn14Thr
NM_002755.3:c.569A>C , LRG_725t1:c.569A>C	NP_002746.1:p.Asp190Ala
XM_011521783.1:c.503A>C	XP_011520085.1:p.Asp168Ala
XM_011521783.3:c.503A>C	XP_011520085.1:p.Asp168Ala
XM_017022411.2:c.491A>C	XP_016877900.1:p.Asp164Ala
XM_017022412.1:c.425A>C	XP_016877901.1:p.Asp142Ala
XM_017022413.1:c.41A>C	XP_016877902.1:p.Asn14Thr
NM_002755.4:c.569A>C MANE Select	NP_002746.1:p.Asp190Ala