Canonical Allele Identifier: CA402507035

Gene: DYM

Linked Data

• MyVariant Identifiers: chr18:g.46645145G>C (hg19) ; chr18:g.49118775G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49118775G>C , CM000680.2:g.49118775G>C	GRCh38
NC_000018.9:g.46645145G>C , CM000680.1:g.46645145G>C	GRCh37
NC_000018.8:g.44899143G>C	NCBI36
NG_009239.1:g.346935C>G
NG_009239.2:g.346959C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000675505.1:c.1880C>G MANE Select	ENSP00000501694.1:p.Ser627Ter
ENST00000269445.10:c.1715C>G	ENSP00000269445.6:p.Ser572Ter
ENST00000442713.6:c.1145C>G	ENSP00000395942.2:p.Ser382Ter
NM_017653.3:c.1715C>G	NP_060123.3:p.Ser572Ter
XM_006722488.2:c.1715C>G	XP_006722551.1:p.Ser572Ter
XM_006722490.2:c.1715C>G	XP_006722553.1:p.Ser572Ter
XM_011526036.1:c.1715C>G	XP_011524338.1:p.Ser572Ter
XM_011526037.1:c.1712C>G	XP_011524339.1:p.Ser571Ter
XM_011526038.1:c.1712C>G	XP_011524340.1:p.Ser571Ter
XM_011526039.1:c.1715C>G	XP_011524341.1:p.Ser572Ter
XM_011526040.1:c.1547C>G	XP_011524342.1:p.Ser516Ter
XM_011526041.1:c.1564-21260C>G	XP_011524343.1:n.1564-21260C>G
XM_011526042.1:c.1715C>G	XP_011524344.1:p.Ser572Ter
XM_011526043.1:c.1715C>G	XP_011524345.1:p.Ser572Ter
NM_001353210.1:c.1712C>G	NP_001340139.1:p.Ser571Ter
NM_001353211.1:c.1712C>G	NP_001340140.1:p.Ser571Ter
NM_001353212.1:c.1877C>G	NP_001340141.1:p.Ser626Ter
NM_001353213.1:c.1877C>G	NP_001340142.1:p.Ser626Ter
NM_001353214.1:c.1880C>G	NP_001340143.1:p.Ser627Ter
NM_001353215.1:c.1729-21260C>G	NP_001340144.1:n.1729-21260C>G
NM_001353216.1:c.1564-21260C>G	NP_001340145.1:n.1564-21260C>G
NM_017653.4:c.1715C>G	NP_060123.3:p.Ser572Ter
XM_006722488.3:c.1715C>G	XP_006722551.1:p.Ser572Ter
XM_011526036.2:c.1715C>G	XP_011524338.1:p.Ser572Ter
XM_011526038.2:c.1712C>G	XP_011524340.1:p.Ser571Ter
XM_011526039.2:c.1715C>G	XP_011524341.1:p.Ser572Ter
XM_011526041.2:c.1564-21260C>G	XP_011524343.1:n.1564-21260C>G
XM_011526042.2:c.1715C>G	XP_011524344.1:p.Ser572Ter
XM_017025795.1:c.1709C>G	XP_016881284.1:p.Ser570Ter
XM_017025796.2:c.1535C>G	XP_016881285.1:p.Ser512Ter
XM_017025800.2:c.1561-21260C>G	XP_016881289.1:n.1561-21260C>G
XM_017025801.1:c.1558-21260C>G	XP_016881290.1:n.1558-21260C>G
XR_002958177.1:n.2072C>G
NM_001353210.3:c.1712C>G	NP_001340139.1:p.Ser571Ter
NM_001353211.3:c.1712C>G	NP_001340140.1:p.Ser571Ter
NM_001353212.3:c.1877C>G	NP_001340141.1:p.Ser626Ter
NM_001353213.3:c.1877C>G	NP_001340142.1:p.Ser626Ter
NM_001353214.3:c.1880C>G MANE Select	NP_001340143.1:p.Ser627Ter
NM_001353215.3:c.1729-21260C>G	NP_001340144.1:n.1729-21260C>G
NM_001353216.3:c.1564-21260C>G	NP_001340145.1:n.1564-21260C>G
NM_001374428.1:c.1880C>G	NP_001361357.1:p.Ser627Ter
NM_001374429.1:c.1874C>G	NP_001361358.1:p.Ser625Ter
NM_001374430.1:c.1880C>G	NP_001361359.1:p.Ser627Ter
NM_001374431.1:c.1880C>G	NP_001361360.1:p.Ser627Ter
NM_001374432.1:c.1754C>G	NP_001361361.1:p.Ser585Ter
NM_001374433.1:c.1715C>G	NP_001361362.1:p.Ser572Ter
NM_001374434.1:c.1715C>G	NP_001361363.1:p.Ser572Ter
NM_001374435.1:c.1712C>G	NP_001361364.1:p.Ser571Ter
NM_001374436.1:c.1589C>G	NP_001361365.1:p.Ser530Ter
NM_001374437.1:c.1532C>G	NP_001361366.1:p.Ser511Ter
NM_001374438.1:c.1561-21260C>G	NP_001361367.1:n.1561-21260C>G
NM_001374439.1:c.1558-21260C>G	NP_001361368.1:n.1558-21260C>G
NM_001374440.1:c.1487C>G	NP_001361369.1:p.Ser496Ter
NM_001374441.1:c.1310C>G	NP_001361370.1:p.Ser437Ter
NM_001374442.1:c.1145C>G	NP_001361371.1:p.Ser382Ter
NM_001374443.1:c.1142C>G	NP_001361372.1:p.Ser381Ter
NM_001374444.1:c.994-21260C>G	NP_001361373.1:n.994-21260C>G
NM_017653.6:c.1715C>G	NP_060123.3:p.Ser572Ter