Canonical Allele Identifier: CA2338362313
Gene: MARK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45303351A>C , CM000681.2:g.45303351A>C GRCh38
NC_000019.9:g.45806609A>C , CM000681.1:g.45806609A>C GRCh37
NC_000019.8:g.50498449A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262891.9:c.*641A>C MANE Select ENSP00000262891.3:n.*641A>C
ENST00000262891.8:c.*641A>C ENSP00000262891.3:n.*641A>C
ENST00000300843.8:c.*913A>C ENSP00000300843.3:n.*913A>C
ENST00000620044.4:c.*1279A>C ENSP00000480702.1:n.*1279A>C
ENST00000622871.1:c.*641A>C ENSP00000484974.1:n.*641A>C
NM_001199867.1:c.*641A>C NP_001186796.1:n.*641A>C
NM_031417.3:c.*913A>C NP_113605.2:n.*913A>C
XM_006723307.2:c.*641A>C XP_006723370.1:n.*641A>C
XM_006723307.4:c.*641A>C XP_006723370.1:n.*641A>C
NM_001199867.2:c.*641A>C MANE Select NP_001186796.1:n.*641A>C
NM_031417.4:c.*913A>C NP_113605.2:n.*913A>C