Canonical Allele Identifier: CA272673637

Gene: MAP2K5

Linked Data

• dbSNP Id: rs548069885
• MyVariant Identifiers: chr15:g.68086789T>C (hg19) ; chr15:g.67794451T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67794451T>C , CM000677.2:g.67794451T>C	GRCh38
NC_000015.9:g.68086789T>C , CM000677.1:g.68086789T>C	GRCh37
NC_000015.8:g.65873843T>C	NCBI36
NG_029143.1:g.256769T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000178640.10:c.1243-12195T>C MANE Select	ENSP00000178640.5:n.1243-12195T>C
ENST00000178640.9:c.1243-12195T>C	ENSP00000178640.5:n.1243-12195T>C
ENST00000340972.8:c.673-12195T>C	ENSP00000342101.4:n.673-12195T>C
ENST00000354498.9:c.1135-12195T>C	ENSP00000346493.5:n.1135-12195T>C
ENST00000395476.6:c.1213-12195T>C	ENSP00000378859.2:n.1213-12195T>C
ENST00000558274.1:n.327-12195T>C
ENST00000558392.5:n.1069-12195T>C
NM_001206804.1:c.1135-12195T>C	NP_001193733.1:n.1135-12195T>C
NM_002757.3:c.1213-12195T>C	NP_002748.1:n.1213-12195T>C
NM_145160.2:c.1243-12195T>C	NP_660143.1:n.1243-12195T>C
XM_011521784.1:c.1288-12195T>C	XP_011520086.1:n.1288-12195T>C
XM_011521786.1:c.1216-12195T>C	XP_011520088.1:n.1216-12195T>C
XM_024449988.1:c.1012-12195T>C	XP_024305756.1:n.1012-12195T>C
NM_145160.3:c.1243-12195T>C MANE Select	NP_660143.1:n.1243-12195T>C
NM_001206804.2:c.1135-12195T>C	NP_001193733.1:n.1135-12195T>C
NM_002757.4:c.1213-12195T>C	NP_002748.1:n.1213-12195T>C