Canonical Allele Identifier: CA2570363600

Gene: DYNC2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103220620_103220621insG , CM000673.2:g.103220620_103220621insG	GRCh38
NC_000011.9:g.103091349_103091350insG , CM000673.1:g.103091349_103091350insG	GRCh37
NC_000011.8:g.102596559_102596560insG	NCBI36
NG_016423.1:g.116190_116191insG
NG_016423.2:g.116190_116191insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.8947-3_8947-2insG MANE Plus Clinical	ENSP00000497174.1:n.8947-3_8947-2insG
ENST00000375735.7:c.8947-3_8947-2insG MANE Select	ENSP00000364887.2:n.8947-3_8947-2insG
ENST00000650373.1:c.8947-3_8947-2insG	ENSP00000497174.1:n.8947-3_8947-2insG
ENST00000334267.11:c.2205+86201_2205+86202insG	ENSP00000334021.7:n.2205+86201_2205+86202insG
ENST00000375735.6:c.8947-3_8947-2insG	ENSP00000364887.2:n.8947-3_8947-2insG
ENST00000398093.7:c.8947-3_8947-2insG	ENSP00000381167.3:n.8947-3_8947-2insG
NM_001080463.1:c.8947-3_8947-2insG	NP_001073932.1:n.8947-3_8947-2insG
NM_001377.2:c.8947-3_8947-2insG	NP_001368.2:n.8947-3_8947-2insG
XM_006718903.2:c.8926-3_8926-2insG	XP_006718966.1:n.8926-3_8926-2insG
XM_017018291.1:c.8947-3_8947-2insG	XP_016873780.1:n.8947-3_8947-2insG
XM_017018292.1:c.8329-3_8329-2insG	XP_016873781.1:n.8329-3_8329-2insG
NM_001377.3:c.8947-3_8947-2insG MANE Select	NP_001368.2:n.8947-3_8947-2insG
NM_001080463.2:c.8947-3_8947-2insG MANE Plus Clinical	NP_001073932.1:n.8947-3_8947-2insG