Canonical Allele Identifier: CA223804824
Gene: MARK2 HGNC NCBI

Linked Data

dbSNP Id: rs12099085

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.63899472C>T , CM000673.2:g.63899472C>T GRCh38
NC_000011.9:g.63666944C>T , CM000673.1:g.63666944C>T GRCh37
NC_000011.8:g.63423520C>T NCBI36
NG_029771.1:g.65545C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707173.1:c.432+364C>T ENSP00000516773.1:n.432+364C>T
ENST00000377810.8:c.531+364C>T ENSP00000367041.5:n.531+364C>T
ENST00000402010.8:c.531+364C>T MANE Select ENSP00000385751.2:n.531+364C>T
ENST00000425897.3:c.531+364C>T ENSP00000415494.3:n.531+364C>T
ENST00000513765.7:c.531+364C>T ENSP00000421075.3:n.531+364C>T
ENST00000676602.1:n.2922+364C>T
ENST00000677688.1:c.432+364C>T ENSP00000503547.1:n.432+364C>T
ENST00000678482.1:n.2941+364C>T
ENST00000678662.1:n.388+364C>T
ENST00000679216.1:c.531+364C>T ENSP00000504337.1:n.531+364C>T
ENST00000679321.1:n.813C>T
ENST00000350490.11:c.531+364C>T ENSP00000294247.9:n.531+364C>T
ENST00000361128.9:c.531+364C>T ENSP00000355091.5:n.531+364C>T
ENST00000377810.7:c.432+364C>T ENSP00000367041.4:n.432+364C>T
ENST00000402010.6:c.531+364C>T ENSP00000385751.2:n.531+364C>T
ENST00000408948.7:c.432+364C>T ENSP00000386128.3:n.432+364C>T
ENST00000425897.2:c.432+364C>T ENSP00000415494.2:n.432+364C>T
ENST00000502399.7:c.531+364C>T ENSP00000423452.3:n.531+364C>T
ENST00000508192.5:c.531+364C>T ENSP00000425765.1:n.531+364C>T
ENST00000509502.6:c.432+364C>T ENSP00000423974.2:n.432+364C>T
ENST00000513765.6:c.432+364C>T ENSP00000421075.2:n.432+364C>T
ENST00000543220.5:c.432+364C>T ENSP00000444956.1:n.432+364C>T
NM_001039469.2:c.531+364C>T NP_001034558.2:n.531+364C>T
NM_001163296.1:c.531+364C>T NP_001156768.1:n.531+364C>T
NM_001163297.1:c.531+364C>T NP_001156769.1:n.531+364C>T
NM_004954.4:c.531+364C>T NP_004945.4:n.531+364C>T
NM_017490.3:c.432+364C>T NP_059672.2:n.432+364C>T
XM_011544789.1:c.591+364C>T XP_011543091.1:n.591+364C>T
XM_011544790.1:c.591+364C>T XP_011543092.1:n.591+364C>T
XM_011544791.1:c.591+364C>T XP_011543093.1:n.591+364C>T
XM_011544792.1:c.591+364C>T XP_011543094.1:n.591+364C>T
XM_011544793.1:c.591+364C>T XP_011543095.1:n.591+364C>T
XM_011544794.1:c.591+364C>T XP_011543096.1:n.591+364C>T
XM_011544795.1:c.591+364C>T XP_011543097.1:n.591+364C>T
XM_011544796.1:c.591+364C>T XP_011543098.1:n.591+364C>T
XM_011544797.1:c.591+364C>T XP_011543099.1:n.591+364C>T
XM_011544798.1:c.591+364C>T XP_011543100.1:n.591+364C>T
XR_949801.1:n.895+364C>T
XR_949802.1:n.1083+364C>T
XM_017017310.1:c.531+364C>T XP_016872799.1:n.531+364C>T
XM_017017311.1:c.591+364C>T XP_016872800.1:n.591+364C>T
XR_002957128.1:n.1001+364C>T
XR_949801.2:n.541+364C>T
XR_949802.2:n.1083+364C>T
NM_001163296.2:c.531+364C>T NP_001156768.1:n.531+364C>T
NM_001163297.2:c.531+364C>T NP_001156769.1:n.531+364C>T
NM_004954.5:c.531+364C>T NP_004945.4:n.531+364C>T
NM_017490.4:c.432+364C>T NP_059672.2:n.432+364C>T
NM_001039469.3:c.531+364C>T MANE Select NP_001034558.2:n.531+364C>T