Canonical Allele Identifier: CA32960828
Gene: DNM3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172230433T>A , CM000663.2:g.172230433T>A GRCh38
NC_000001.10:g.172199573T>A , CM000663.1:g.172199573T>A GRCh37
NC_000001.9:g.170466196T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000485254.3:c.1690-23140T>A ENSP00000429165.2:n.1690-23140T>A
ENST00000688173.1:c.1330-23140T>A ENSP00000509172.1:n.1330-23140T>A
ENST00000627582.3:c.1660-23140T>A MANE Select ENSP00000486701.1:n.1660-23140T>A
ENST00000355305.9:c.1690-23140T>A ENSP00000347457.5:n.1690-23140T>A
ENST00000367731.5:c.1660-23140T>A ENSP00000356705.1:n.1660-23140T>A
ENST00000520906.5:c.1660-23140T>A ENSP00000429701.1:n.1660-23140T>A
ENST00000523513.1:c.1330-23140T>A ENSP00000429416.1:n.1330-23140T>A
ENST00000627582.2:c.1660-23140T>A ENSP00000486701.1:n.1660-23140T>A
NM_001136127.2:c.1660-23140T>A NP_001129599.1:n.1660-23140T>A
NM_015569.4:c.1660-23140T>A NP_056384.2:n.1660-23140T>A
XM_005245079.1:c.1690-23140T>A XP_005245136.1:n.1690-23140T>A
XM_005245080.1:c.1690-23140T>A XP_005245137.1:n.1690-23140T>A
XM_005245081.1:c.1690-23140T>A XP_005245138.1:n.1690-23140T>A
XM_005245082.3:c.1360-23140T>A XP_005245139.1:n.1360-23140T>A
XM_005245084.3:c.1690-23140T>A XP_005245141.1:n.1690-23140T>A
XM_011509400.1:c.1690-23140T>A XP_011507702.1:n.1690-23140T>A
XM_011509401.1:c.1690-23140T>A XP_011507703.1:n.1690-23140T>A
NM_001350204.1:c.1690-23140T>A NP_001337133.1:n.1690-23140T>A
NM_001350206.1:c.1690-23140T>A NP_001337135.1:n.1690-23140T>A
NR_146559.1:n.1885-23140T>A
XM_017000976.1:c.1834-23140T>A XP_016856465.1:n.1834-23140T>A
XM_017000977.1:c.1834-23140T>A XP_016856466.1:n.1834-23140T>A
XM_017000978.1:c.1804-23140T>A XP_016856467.1:n.1804-23140T>A
XM_017000979.1:c.1834-23140T>A XP_016856468.1:n.1834-23140T>A
XM_017000980.1:c.1705-23140T>A XP_016856469.1:n.1705-23140T>A
XM_017000982.2:c.1690-23140T>A XP_016856471.1:n.1690-23140T>A
XM_017000983.1:c.1660-23140T>A XP_016856472.1:n.1660-23140T>A
XM_017000984.1:c.1660-23140T>A XP_016856473.1:n.1660-23140T>A
XM_017000985.1:c.1660-23140T>A XP_016856474.1:n.1660-23140T>A
XM_017000986.1:c.1561-23140T>A XP_016856475.1:n.1561-23140T>A
XM_017000987.1:c.1360-23140T>A XP_016856476.1:n.1360-23140T>A
XM_017000991.1:c.*11-78295T>A XP_016856480.1:n.*11-78295T>A
XR_001737107.1:n.1852-78295T>A
XR_001737108.1:n.1868-23140T>A
XR_001737110.1:n.1822-78295T>A
XR_001737111.1:n.1580-23140T>A
NM_015569.5:c.1660-23140T>A MANE Select NP_056384.2:n.1660-23140T>A
NM_001136127.3:c.1660-23140T>A NP_001129599.1:n.1660-23140T>A
NM_001350204.2:c.1690-23140T>A NP_001337133.1:n.1690-23140T>A
NM_001350206.2:c.1690-23140T>A NP_001337135.1:n.1690-23140T>A
NR_146559.2:n.1865-23140T>A
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