Canonical Allele Identifier: CA891126551

Gene: DNM3

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171863954C>T , CM000663.2:g.171863954C>T	GRCh38
NC_000001.10:g.171833094C>T , CM000663.1:g.171833094C>T	GRCh37
NC_000001.9:g.170099717C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485254.3:c.161+22137C>T	ENSP00000429165.2:n.161+22137C>T
ENST00000688173.1:c.-96+45911C>T	ENSP00000509172.1:n.-96+45911C>T
ENST00000627582.3:c.161+22137C>T MANE Select	ENSP00000486701.1:n.161+22137C>T
ENST00000355305.9:c.161+22137C>T	ENSP00000347457.5:n.161+22137C>T
ENST00000367731.5:c.161+22137C>T	ENSP00000356705.1:n.161+22137C>T
ENST00000367733.6:c.161+22137C>T	ENSP00000356707.2:n.161+22137C>T
ENST00000520906.5:c.161+22137C>T	ENSP00000429701.1:n.161+22137C>T
ENST00000627582.2:c.161+22137C>T	ENSP00000486701.1:n.161+22137C>T
NM_001136127.2:c.161+22137C>T	NP_001129599.1:n.161+22137C>T
NM_001278252.1:c.161+22137C>T	NP_001265181.1:n.161+22137C>T
NM_015569.4:c.161+22137C>T	NP_056384.2:n.161+22137C>T
XM_005245079.1:c.161+22137C>T	XP_005245136.1:n.161+22137C>T
XM_005245080.1:c.161+22137C>T	XP_005245137.1:n.161+22137C>T
XM_005245081.1:c.161+22137C>T	XP_005245138.1:n.161+22137C>T
XM_005245084.3:c.161+22137C>T	XP_005245141.1:n.161+22137C>T
XM_006711268.2:c.161+22137C>T	XP_006711331.1:n.161+22137C>T
XM_011509400.1:c.161+22137C>T	XP_011507702.1:n.161+22137C>T
XM_011509401.1:c.161+22137C>T	XP_011507703.1:n.161+22137C>T
XM_011509402.1:c.161+22137C>T	XP_011507704.1:n.161+22137C>T
NM_001350204.1:c.161+22137C>T	NP_001337133.1:n.161+22137C>T
NM_001350205.1:c.161+22137C>T	NP_001337134.1:n.161+22137C>T
NM_001350206.1:c.161+22137C>T	NP_001337135.1:n.161+22137C>T
NR_146559.1:n.340+22137C>T
XM_017000976.1:c.161+22137C>T	XP_016856465.1:n.161+22137C>T
XM_017000977.1:c.161+22137C>T	XP_016856466.1:n.161+22137C>T
XM_017000978.1:c.161+22137C>T	XP_016856467.1:n.161+22137C>T
XM_017000979.1:c.161+22137C>T	XP_016856468.1:n.161+22137C>T
XM_017000982.2:c.161+22137C>T	XP_016856471.1:n.161+22137C>T
XM_017000983.1:c.161+22137C>T	XP_016856472.1:n.161+22137C>T
XM_017000984.1:c.161+22137C>T	XP_016856473.1:n.161+22137C>T
XM_017000985.1:c.161+22137C>T	XP_016856474.1:n.161+22137C>T
XM_017000988.1:c.161+22137C>T	XP_016856477.1:n.161+22137C>T
XM_017000989.1:c.161+22137C>T	XP_016856478.1:n.161+22137C>T
XM_017000990.2:c.161+22137C>T	XP_016856479.1:n.161+22137C>T
XM_017000991.1:c.161+22137C>T	XP_016856480.1:n.161+22137C>T
XM_017000992.1:c.161+22137C>T	XP_016856481.1:n.161+22137C>T
XR_001737107.1:n.323+22137C>T
XR_001737108.1:n.323+22137C>T
XR_001737110.1:n.323+22137C>T
NM_015569.5:c.161+22137C>T MANE Select	NP_056384.2:n.161+22137C>T
NM_001136127.3:c.161+22137C>T	NP_001129599.1:n.161+22137C>T
NM_001278252.2:c.161+22137C>T	NP_001265181.1:n.161+22137C>T
NM_001350204.2:c.161+22137C>T	NP_001337133.1:n.161+22137C>T
NM_001350205.2:c.161+22137C>T	NP_001337134.1:n.161+22137C>T
NM_001350206.2:c.161+22137C>T	NP_001337135.1:n.161+22137C>T
NR_146559.2:n.320+22137C>T