Canonical Allele Identifier: CA8958023

Gene: DYM

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49118893G>A , CM000680.2:g.49118893G>A	GRCh38
NC_000018.9:g.46645263G>A , CM000680.1:g.46645263G>A	GRCh37
NC_000018.8:g.44899261G>A	NCBI36
NG_009239.1:g.346817C>T
NG_009239.2:g.346841C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001353214.3:c.1762C>T MANE Select	NP_001340143.1:p.Arg588Ter
ENST00000675505.1:c.1762C>T MANE Select	ENSP00000501694.1:p.Arg588Ter
NM_001353210.1:c.1594C>T	NP_001340139.1:p.Arg532Ter
NM_001353210.3:c.1594C>T	NP_001340139.1:p.Arg532Ter
NM_001353211.1:c.1594C>T	NP_001340140.1:p.Arg532Ter
NM_001353211.3:c.1594C>T	NP_001340140.1:p.Arg532Ter
NM_001353212.1:c.1759C>T	NP_001340141.1:p.Arg587Ter
NM_001353212.3:c.1759C>T	NP_001340141.1:p.Arg587Ter
NM_001353213.1:c.1759C>T	NP_001340142.1:p.Arg587Ter
NM_001353213.3:c.1759C>T	NP_001340142.1:p.Arg587Ter
NM_001353214.1:c.1762C>T	NP_001340143.1:p.Arg588Ter
NM_001353215.1:c.1729-21378C>T	NP_001340144.1:n.1729-21378C>T
NM_001353215.3:c.1729-21378C>T	NP_001340144.1:n.1729-21378C>T
NM_001353216.1:c.1564-21378C>T	NP_001340145.1:n.1564-21378C>T
NM_001353216.3:c.1564-21378C>T	NP_001340145.1:n.1564-21378C>T
NM_001374428.1:c.1762C>T	NP_001361357.1:p.Arg588Ter
NM_001374429.1:c.1756C>T	NP_001361358.1:p.Arg586Ter
NM_001374430.1:c.1762C>T	NP_001361359.1:p.Arg588Ter
NM_001374431.1:c.1762C>T	NP_001361360.1:p.Arg588Ter
NM_001374432.1:c.1636C>T	NP_001361361.1:p.Arg546Ter
NM_001374433.1:c.1597C>T	NP_001361362.1:p.Arg533Ter
NM_001374434.1:c.1597C>T	NP_001361363.1:p.Arg533Ter
NM_001374435.1:c.1594C>T	NP_001361364.1:p.Arg532Ter
NM_001374436.1:c.1471C>T	NP_001361365.1:p.Arg491Ter
NM_001374437.1:c.1414C>T	NP_001361366.1:p.Arg472Ter
NM_001374438.1:c.1561-21378C>T	NP_001361367.1:n.1561-21378C>T
NM_001374439.1:c.1558-21378C>T	NP_001361368.1:n.1558-21378C>T
NM_001374440.1:c.1369C>T	NP_001361369.1:p.Arg457Ter
NM_001374441.1:c.1192C>T	NP_001361370.1:p.Arg398Ter
NM_001374442.1:c.1027C>T	NP_001361371.1:p.Arg343Ter
NM_001374443.1:c.1024C>T	NP_001361372.1:p.Arg342Ter
NM_001374444.1:c.994-21378C>T	NP_001361373.1:n.994-21378C>T
NM_017653.3:c.1597C>T	NP_060123.3:p.Arg533Ter
NM_017653.4:c.1597C>T	NP_060123.3:p.Arg533Ter
NM_017653.6:c.1597C>T	NP_060123.3:p.Arg533Ter
ENST00000269445.10:c.1597C>T	ENSP00000269445.6:p.Arg533Ter
ENST00000442713.6:c.1027C>T	ENSP00000395942.2:p.Arg343Ter
XM_006722488.2:c.1597C>T	XP_006722551.1:p.Arg533Ter
XM_006722488.3:c.1597C>T	XP_006722551.1:p.Arg533Ter
XM_006722490.2:c.1597C>T	XP_006722553.1:p.Arg533Ter
XM_011526036.1:c.1597C>T	XP_011524338.1:p.Arg533Ter
XM_011526036.2:c.1597C>T	XP_011524338.1:p.Arg533Ter
XM_011526037.1:c.1594C>T	XP_011524339.1:p.Arg532Ter
XM_011526038.1:c.1594C>T	XP_011524340.1:p.Arg532Ter
XM_011526038.2:c.1594C>T	XP_011524340.1:p.Arg532Ter
XM_011526039.1:c.1597C>T	XP_011524341.1:p.Arg533Ter
XM_011526039.2:c.1597C>T	XP_011524341.1:p.Arg533Ter
XM_011526040.1:c.1429C>T	XP_011524342.1:p.Arg477Ter
XM_011526041.1:c.1564-21378C>T	XP_011524343.1:n.1564-21378C>T
XM_011526041.2:c.1564-21378C>T	XP_011524343.1:n.1564-21378C>T
XM_011526042.1:c.1597C>T	XP_011524344.1:p.Arg533Ter
XM_011526042.2:c.1597C>T	XP_011524344.1:p.Arg533Ter
XM_011526043.1:c.1597C>T	XP_011524345.1:p.Arg533Ter
XM_017025795.1:c.1591C>T	XP_016881284.1:p.Arg531Ter
XM_017025796.2:c.1417C>T	XP_016881285.1:p.Arg473Ter
XM_017025800.2:c.1561-21378C>T	XP_016881289.1:n.1561-21378C>T
XM_017025801.1:c.1558-21378C>T	XP_016881290.1:n.1558-21378C>T
XR_002958177.1:n.1954C>T