Canonical Allele Identifier: CA101347629

Gene: MAPK10

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.86552623G>A , CM000666.2:g.86552623G>A	GRCh38
NC_000004.11:g.87473776G>A , CM000666.1:g.87473776G>A	GRCh37
NC_000004.10:g.87692800G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502302.6:c.-263+41287C>T	ENSP00000423918.2:n.-263+41287C>T
ENST00000506773.7:n.165+41287C>T
ENST00000512046.2:c.-122+41110C>T	ENSP00000492508.1:n.-122+41110C>T
ENST00000513186.7:c.-122+41287C>T	ENSP00000420987.3:n.-122+41287C>T
ENST00000515400.3:c.-159+41287C>T	ENSP00000424154.3:n.-159+41287C>T
ENST00000640527.1:c.-276+41287C>T	ENSP00000491389.1:n.-276+41287C>T
ENST00000641050.1:c.-274+41287C>T	ENSP00000493270.1:n.-274+41287C>T
ENST00000641051.1:c.-274+41287C>T	ENSP00000493275.1:n.-274+41287C>T
ENST00000641157.1:c.-182+41287C>T	ENSP00000493363.1:n.-182+41287C>T
ENST00000641391.1:c.-300+41287C>T	ENSP00000493008.1:n.-300+41287C>T
ENST00000641737.1:c.-415+41287C>T	ENSP00000493177.1:n.-415+41287C>T
ENST00000641831.1:c.-428+41110C>T	ENSP00000492886.1:n.-428+41110C>T
ENST00000502302.5:c.-263+41287C>T	ENSP00000423918.1:n.-263+41287C>T
ENST00000512046.1:n.387+41110C>T
ENST00000513186.5:c.-122+41287C>T	ENSP00000420987.1:n.-122+41287C>T
ENST00000513839.5:n.201+41287C>T
XM_011532117.1:c.-122+41287C>T	XP_011530419.1:n.-122+41287C>T
XM_011532120.1:c.-263+41287C>T	XP_011530422.1:n.-263+41287C>T
XM_011532117.3:c.-122+41287C>T	XP_011530419.1:n.-122+41287C>T
XM_011532120.3:c.-263+41287C>T	XP_011530422.1:n.-263+41287C>T
XM_017008428.2:c.-263+41287C>T	XP_016863917.1:n.-263+41287C>T
XM_017008454.2:c.-122+41287C>T	XP_016863943.1:n.-122+41287C>T
XM_024454141.1:c.-274+41287C>T	XP_024309909.1:n.-274+41287C>T
XM_024454142.1:c.-182+41287C>T	XP_024309910.1:n.-182+41287C>T
XM_024454144.1:c.-274+41287C>T	XP_024309912.1:n.-274+41287C>T
XM_024454145.1:c.-122+41287C>T	XP_024309913.1:n.-122+41287C>T