Canonical Allele Identifier: CA2184571496

Gene: MAP2K5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67543173T= , CM000677.2:g.67543173T=	GRCh38
NC_000015.9:g.67835511T= , CM000677.1:g.67835511T=	GRCh37
NC_000015.8:g.65622565T=	NCBI36
NG_029143.1:g.5491T=

Transcript Alleles

HGVS	Amino-acid Change
NM_145160.3:c.-163T= MANE Select	NP_660143.1:n.-163T=
ENST00000178640.10:c.-163T= MANE Select	ENSP00000178640.5:n.-163T=
NM_002757.3:c.-163T=	NP_002748.1:n.-163T=
NM_002757.4:c.-163T=	NP_002748.1:n.-163T=
NM_145160.2:c.-163T=	NP_660143.1:n.-163T=
ENST00000178640.9:c.-163T=	ENSP00000178640.5:n.-163T=
XM_011521784.1:c.-163T=	XP_011520086.1:n.-163T=
XM_011521785.1:c.-163T=	XP_011520087.1:n.-163T=
XM_011521786.1:c.-163T=	XP_011520088.1:n.-163T=
XM_011521787.1:c.-163T=	XP_011520089.1:n.-163T=
XM_011521787.3:c.-163T=	XP_011520089.1:n.-163T=
XM_011521788.1:c.-163T=	XP_011520090.1:n.-163T=
XM_011521788.3:c.-163T=	XP_011520090.1:n.-163T=
XM_017022414.2:c.-163T=	XP_016877903.1:n.-163T=
XM_024449988.1:c.-801T=	XP_024305756.1:n.-801T=
XR_001751355.2:n.489T=