Canonical Allele Identifier: CA2319219616

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090423_4090424delinsCG , CM000681.2:g.4090423_4090424delinsCG	GRCh38
NC_000019.9:g.4090421_4090422delinsCG , CM000681.1:g.4090421_4090422delinsCG	GRCh37
NC_000019.8:g.4041421_4041422delinsCG	NCBI36
NG_007996.1:g.38705_38706delinsCG , LRG_750:g.38705_38706delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1816_1817delinsCG
ENST00000688751.1:n.513_514delinsCG
ENST00000689792.1:n.1281_1282delinsCG
ENST00000262948.10:c.*174_*175delinsCG MANE Select	ENSP00000262948.4:n.*174_*175delinsCG
ENST00000262948.9:c.*174_*175delinsCG	ENSP00000262948.3:n.*174_*175delinsCG
ENST00000394867.8:c.*174_*175delinsCG	ENSP00000378336.1:n.*174_*175delinsCG
ENST00000600584.5:n.2826_2827delinsCG
ENST00000601786.5:n.1678_1679delinsCG
NM_030662.3:c.*174_*175delinsCG , LRG_750t1:c.*174_*175delinsCG	NP_109587.1:n.*174_*175delinsCG
XM_006722799.2:c.*174_*175delinsCG	XP_006722862.1:n.*174_*175delinsCG
XM_011528133.1:c.*174_*175delinsCG	XP_011526435.1:n.*174_*175delinsCG
NM_030662.4:c.*174_*175delinsCG MANE Select	NP_109587.1:n.*174_*175delinsCG