Canonical Allele Identifier: CA1139991104
Gene: MARK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220652181A= , CM000663.2:g.220652181A= GRCh38
NC_000001.10:g.220825523A= , CM000663.1:g.220825523A= GRCh37
NC_000001.9:g.218892146A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_018650.5:c.1736+31A= MANE Select NP_061120.3:n.1736+31A=
ENST00000366917.6:c.1736+31A= MANE Select ENSP00000355884.5:n.1736+31A=
NM_001286124.1:c.1736+31A= NP_001273053.1:n.1736+31A=
NM_001286124.2:c.1736+31A= NP_001273053.1:n.1736+31A=
NM_001286126.1:c.1736+31A= NP_001273055.1:n.1736+31A=
NM_001286126.2:c.1736+31A= NP_001273055.1:n.1736+31A=
NM_001286128.1:c.1670+31A= NP_001273057.1:n.1670+31A=
NM_001286128.2:c.1670+31A= NP_001273057.1:n.1670+31A=
NM_018650.4:c.1736+31A= NP_061120.3:n.1736+31A=
ENST00000366917.5:c.1736+31A= ENSP00000355884.4:n.1736+31A=
ENST00000366918.8:c.1670+31A= ENSP00000355885.4:n.1670+31A=
ENST00000402574.5:c.1736+31A= ENSP00000386017.2:n.1736+31A=
ENST00000611084.4:c.1736+31A= ENSP00000483424.1:n.1736+31A=
ENST00000677041.1:c.*1659+31A= ENSP00000504826.1:n.*1659+31A=
ENST00000677074.1:n.2924+31A=
ENST00000677505.1:c.1670+31A= ENSP00000504370.1:n.1670+31A=
ENST00000678435.1:c.1406+31A= ENSP00000503257.1:n.1406+31A=
XM_005273134.3:c.1736+31A= XP_005273191.1:n.1736+31A=
XM_005273134.5:c.1736+31A= XP_005273191.1:n.1736+31A=
XM_006711326.2:c.1472+31A= XP_006711389.1:n.1472+31A=
XM_006711326.4:c.1472+31A= XP_006711389.1:n.1472+31A=
XM_006711327.2:c.1244+31A= XP_006711390.1:n.1244+31A=
XM_011509561.1:c.1712+31A= XP_011507863.1:n.1712+31A=
XM_011509561.3:c.1712+31A= XP_011507863.1:n.1712+31A=
XM_011509562.1:c.1406+31A= XP_011507864.1:n.1406+31A=
XM_011509562.3:c.1406+31A= XP_011507864.1:n.1406+31A=
XM_017001305.2:c.1406+31A= XP_016856794.1:n.1406+31A=
XM_017001306.2:c.1406+31A= XP_016856795.1:n.1406+31A=
XM_017001307.2:c.1406+31A= XP_016856796.1:n.1406+31A=