Canonical Allele Identifier: CA288518715
Gene: MAPK7 HGNC NCBI

Linked Data

dbSNP Id: rs1042865
MyVariant Identifiers: chr17:g.19286605C>T (hg19) chr17:g.19383292C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19383292C>T , CM000679.2:g.19383292C>T GRCh38
NC_000017.10:g.19286605C>T , CM000679.1:g.19286605C>T GRCh37
NC_000017.9:g.19227198C>T NCBI36
NG_027952.1:g.8928G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395604.8:c.*61C>T MANE Select ENSP00000378968.3:n.*61C>T
ENST00000299612.11:c.*61C>T ENSP00000299612.7:n.*61C>T
ENST00000308406.9:c.*61C>T ENSP00000311005.5:n.*61C>T
ENST00000395602.8:c.*61C>T ENSP00000378966.4:n.*61C>T
ENST00000395604.7:c.*61C>T ENSP00000378968.3:n.*61C>T
ENST00000490660.2:n.2615C>T
ENST00000570306.5:n.4287C>T
ENST00000571657.5:n.652C>T
NM_002749.3:c.*61C>T NP_002740.2:n.*61C>T
NM_139032.2:c.*61C>T NP_620601.1:n.*61C>T
NM_139033.2:c.*61C>T NP_620602.2:n.*61C>T
NM_139034.2:c.*61C>T NP_620603.2:n.*61C>T
XM_005256719.2:c.*61C>T XP_005256776.1:n.*61C>T
XM_006721557.2:c.*61C>T XP_006721620.1:n.*61C>T
XM_006721558.2:c.*61C>T XP_006721621.1:n.*61C>T
XM_006721559.2:c.*61C>T XP_006721622.1:n.*61C>T
XM_011523957.1:c.*61C>T XP_011522259.1:n.*61C>T
XM_006721557.3:c.*61C>T XP_006721620.1:n.*61C>T
XM_006721558.3:c.*61C>T XP_006721621.1:n.*61C>T
XM_006721559.3:c.*61C>T XP_006721622.1:n.*61C>T
XM_011523957.3:c.*61C>T XP_011522259.1:n.*61C>T
NM_002749.4:c.*61C>T MANE Select NP_002740.2:n.*61C>T
NM_139032.3:c.*61C>T NP_620601.1:n.*61C>T
NM_139034.3:c.*61C>T NP_620603.2:n.*61C>T
NM_139033.3:c.*61C>T NP_620602.2:n.*61C>T
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