Canonical Allele Identifier: CA402506486

Gene: DYM

Linked Data

• dbSNP Id: rs1419961562
• gnomAD v2: 18-46783382-G-C
• gnomAD v4: 18-49257012-G-C
• MyVariant Identifiers: chr18:g.46783382G>C (hg19) ; chr18:g.49257012G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49257012G>C , CM000680.2:g.49257012G>C	GRCh38
NC_000018.9:g.46783382G>C , CM000680.1:g.46783382G>C	GRCh37
NC_000018.8:g.45037380G>C	NCBI36
NG_009239.1:g.208698C>G
NG_009239.2:g.208722C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675505.1:c.1458C>G MANE Select	ENSP00000501694.1:p.Ile486Met
ENST00000269445.10:c.1458C>G	ENSP00000269445.6:p.Ile486Met
ENST00000442713.6:c.888C>G	ENSP00000395942.2:p.Ile296Met
ENST00000582399.1:c.122C>G
NM_017653.3:c.1458C>G	NP_060123.3:p.Ile486Met
XM_006722488.2:c.1458C>G	XP_006722551.1:p.Ile486Met
XM_006722490.2:c.1458C>G	XP_006722553.1:p.Ile486Met
XM_006722491.1:c.1458C>G	XP_006722554.1:p.Ile486Met
XM_006722492.2:c.1458C>G	XP_006722555.1:p.Ile486Met
XM_011526036.1:c.1458C>G	XP_011524338.1:p.Ile486Met
XM_011526037.1:c.1455C>G	XP_011524339.1:p.Ile485Met
XM_011526038.1:c.1455C>G	XP_011524340.1:p.Ile485Met
XM_011526039.1:c.1458C>G	XP_011524341.1:p.Ile486Met
XM_011526040.1:c.1290C>G	XP_011524342.1:p.Ile430Met
XM_011526041.1:c.1458C>G	XP_011524343.1:p.Ile486Met
XM_011526042.1:c.1458C>G	XP_011524344.1:p.Ile486Met
XM_011526043.1:c.1458C>G	XP_011524345.1:p.Ile486Met
NM_001353210.1:c.1455C>G	NP_001340139.1:p.Ile485Met
NM_001353211.1:c.1455C>G	NP_001340140.1:p.Ile485Met
NM_001353212.1:c.1455C>G	NP_001340141.1:p.Ile485Met
NM_001353213.1:c.1455C>G	NP_001340142.1:p.Ile485Met
NM_001353214.1:c.1458C>G	NP_001340143.1:p.Ile486Met
NM_001353215.1:c.1458C>G	NP_001340144.1:p.Ile486Met
NM_001353216.1:c.1458C>G	NP_001340145.1:p.Ile486Met
NM_017653.4:c.1458C>G	NP_060123.3:p.Ile486Met
XM_006722488.3:c.1458C>G	XP_006722551.1:p.Ile486Met
XM_006722492.4:c.1458C>G	XP_006722555.1:p.Ile486Met
XM_011526036.2:c.1458C>G	XP_011524338.1:p.Ile486Met
XM_011526038.2:c.1455C>G	XP_011524340.1:p.Ile485Met
XM_011526039.2:c.1458C>G	XP_011524341.1:p.Ile486Met
XM_011526041.2:c.1458C>G	XP_011524343.1:p.Ile486Met
XM_011526042.2:c.1458C>G	XP_011524344.1:p.Ile486Met
XM_017025795.1:c.1452C>G	XP_016881284.1:p.Ile484Met
XM_017025796.2:c.1278C>G	XP_016881285.1:p.Ile426Met
XM_017025800.2:c.1455C>G	XP_016881289.1:p.Ile485Met
XM_017025801.1:c.1452C>G	XP_016881290.1:p.Ile484Met
XR_002958177.1:n.1815C>G
NM_001353210.3:c.1455C>G	NP_001340139.1:p.Ile485Met
NM_001353211.3:c.1455C>G	NP_001340140.1:p.Ile485Met
NM_001353212.3:c.1455C>G	NP_001340141.1:p.Ile485Met
NM_001353213.3:c.1455C>G	NP_001340142.1:p.Ile485Met
NM_001353214.3:c.1458C>G MANE Select	NP_001340143.1:p.Ile486Met
NM_001353215.3:c.1458C>G	NP_001340144.1:p.Ile486Met
NM_001353216.3:c.1458C>G	NP_001340145.1:p.Ile486Met
NM_001374428.1:c.1458C>G	NP_001361357.1:p.Ile486Met
NM_001374429.1:c.1452C>G	NP_001361358.1:p.Ile484Met
NM_001374430.1:c.1458C>G	NP_001361359.1:p.Ile486Met
NM_001374431.1:c.1458C>G	NP_001361360.1:p.Ile486Met
NM_001374432.1:c.1332C>G	NP_001361361.1:p.Ile444Met
NM_001374433.1:c.1458C>G	NP_001361362.1:p.Ile486Met
NM_001374434.1:c.1458C>G	NP_001361363.1:p.Ile486Met
NM_001374435.1:c.1455C>G	NP_001361364.1:p.Ile485Met
NM_001374436.1:c.1332C>G	NP_001361365.1:p.Ile444Met
NM_001374437.1:c.1275C>G	NP_001361366.1:p.Ile425Met
NM_001374438.1:c.1455C>G	NP_001361367.1:p.Ile485Met
NM_001374439.1:c.1452C>G	NP_001361368.1:p.Ile484Met
NM_001374440.1:c.1230C>G	NP_001361369.1:p.Ile410Met
NM_001374441.1:c.888C>G	NP_001361370.1:p.Ile296Met
NM_001374442.1:c.888C>G	NP_001361371.1:p.Ile296Met
NM_001374443.1:c.885C>G	NP_001361372.1:p.Ile295Met
NM_001374444.1:c.888C>G	NP_001361373.1:p.Ile296Met
NM_017653.6:c.1458C>G	NP_060123.3:p.Ile486Met