Canonical Allele Identifier: CA14508541
Gene: PTPRM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7584296G>A , CM000680.2:g.7584296G>A GRCh38
NC_000018.9:g.7584294G>A , CM000680.1:g.7584294G>A GRCh37
NC_000018.8:g.7574294G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000580170.6:c.73+16405G>A MANE Select ENSP00000463325.1:n.73+16405G>A
ENST00000332175.12:c.73+16405G>A ENSP00000331418.8:n.73+16405G>A
ENST00000580170.5:c.73+16405G>A ENSP00000463325.1:n.73+16405G>A
NM_001105244.1:c.73+16405G>A NP_001098714.1:n.73+16405G>A
NM_002845.3:c.73+16405G>A NP_002836.3:n.73+16405G>A
XM_006722335.2:c.73+16405G>A XP_006722398.1:n.73+16405G>A
XM_006722337.2:c.73+16405G>A XP_006722400.1:n.73+16405G>A
XM_011525708.1:c.73+16405G>A XP_011524010.1:n.73+16405G>A
XM_011525709.1:c.73+16405G>A XP_011524011.1:n.73+16405G>A
XM_011525710.1:c.73+16405G>A XP_011524012.1:n.73+16405G>A
XM_011525711.1:c.73+16405G>A XP_011524013.1:n.73+16405G>A
XM_011525712.1:c.73+16405G>A XP_011524014.1:n.73+16405G>A
XM_011525718.1:c.73+16405G>A XP_011524020.1:n.73+16405G>A
XM_011525719.1:c.73+16405G>A XP_011524021.1:n.73+16405G>A
XM_011525720.1:c.73+16405G>A XP_011524022.1:n.73+16405G>A
XM_011525721.1:c.73+16405G>A XP_011524023.1:n.73+16405G>A
XR_430046.2:n.571+16405G>A
XM_011525708.2:c.73+16405G>A XP_011524010.1:n.73+16405G>A
XM_011525710.2:c.73+16405G>A XP_011524012.1:n.73+16405G>A
XM_011525712.2:c.73+16405G>A XP_011524014.1:n.73+16405G>A
XM_017025911.1:c.73+16405G>A XP_016881400.1:n.73+16405G>A
NM_001105244.2:c.73+16405G>A MANE Select NP_001098714.1:n.73+16405G>A
NM_002845.4:c.73+16405G>A NP_002836.3:n.73+16405G>A
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