Canonical Allele Identifier: CA2184675927

Gene: MAP2K5

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67788548A>C , CM000677.2:g.67788548A>C	GRCh38
NC_000015.9:g.68080886A>C , CM000677.1:g.68080886A>C	GRCh37
NC_000015.8:g.65867940A>C	NCBI36
NG_029143.1:g.250866A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000178640.10:c.1242+15796A>C MANE Select	ENSP00000178640.5:n.1242+15796A>C
ENST00000178640.9:c.1242+15796A>C	ENSP00000178640.5:n.1242+15796A>C
ENST00000340972.8:c.672+15796A>C	ENSP00000342101.4:n.672+15796A>C
ENST00000354498.9:c.1134+15796A>C	ENSP00000346493.5:n.1134+15796A>C
ENST00000395476.6:c.1212+15796A>C	ENSP00000378859.2:n.1212+15796A>C
ENST00000558274.1:n.326+15796A>C
ENST00000558392.5:n.1068+15796A>C
NM_001206804.1:c.1134+15796A>C	NP_001193733.1:n.1134+15796A>C
NM_002757.3:c.1212+15796A>C	NP_002748.1:n.1212+15796A>C
NM_145160.2:c.1242+15796A>C	NP_660143.1:n.1242+15796A>C
XM_011521784.1:c.1287+15796A>C	XP_011520086.1:n.1287+15796A>C
XM_011521786.1:c.1215+15796A>C	XP_011520088.1:n.1215+15796A>C
XM_024449988.1:c.1011+15796A>C	XP_024305756.1:n.1011+15796A>C
NM_145160.3:c.1242+15796A>C MANE Select	NP_660143.1:n.1242+15796A>C
NM_001206804.2:c.1134+15796A>C	NP_001193733.1:n.1134+15796A>C
NM_002757.4:c.1212+15796A>C	NP_002748.1:n.1212+15796A>C