Canonical Allele Identifier: CA2838851124

Gene: DYNC2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103166073_103166074insACCATAGGCCTGAAAGC , CM000673.2:g.103166073_103166074insACCATAGGCCTGAAAGC	GRCh38
NC_000011.9:g.103036802_103036803insACCATAGGCCTGAAAGC , CM000673.1:g.103036802_103036803insACCATAGGCCTGAAAGC	GRCh37
NC_000011.8:g.102542012_102542013insACCATAGGCCTGAAAGC	NCBI36
NG_016423.1:g.61643_61644insACCATAGGCCTGAAAGC
NG_016423.2:g.61643_61644insACCATAGGCCTGAAAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.4762+25_4762+26insACCATAGGCCTGAAAGC MANE Plus Clinical	ENSP00000497174.1:n.4762+25_4762+26insACCATAGGCCTGAAAGC
ENST00000375735.7:c.4762+25_4762+26insACCATAGGCCTGAAAGC MANE Select	ENSP00000364887.2:n.4762+25_4762+26insACCATAGGCCTGAAAGC
ENST00000649323.1:c.*2307+25_*2307+26insACCATAGGCCTGAAAGC	ENSP00000497581.1:n.*2307+25_*2307+26insACCATAGGCCTGAAAGC
ENST00000650373.1:c.4762+25_4762+26insACCATAGGCCTGAAAGC	ENSP00000497174.1:n.4762+25_4762+26insACCATAGGCCTGAAAGC
ENST00000334267.11:c.2205+31654_2205+31655insACCATAGGCCTGAAAGC	ENSP00000334021.7:n.2205+31654_2205+31655insACCATAGGCCTGAAAGC...
ENST00000375735.6:c.4762+25_4762+26insACCATAGGCCTGAAAGC	ENSP00000364887.2:n.4762+25_4762+26insACCATAGGCCTGAAAGC
ENST00000398093.7:c.4762+25_4762+26insACCATAGGCCTGAAAGC	ENSP00000381167.3:n.4762+25_4762+26insACCATAGGCCTGAAAGC
NM_001080463.1:c.4762+25_4762+26insACCATAGGCCTGAAAGC	NP_001073932.1:n.4762+25_4762+26insACCATAGGCCTGAAAGC
NM_001377.2:c.4762+25_4762+26insACCATAGGCCTGAAAGC	NP_001368.2:n.4762+25_4762+26insACCATAGGCCTGAAAGC
XM_006718903.2:c.4762+25_4762+26insACCATAGGCCTGAAAGC	XP_006718966.1:n.4762+25_4762+26insACCATAGGCCTGAAAGC
XM_017018291.1:c.4762+25_4762+26insACCATAGGCCTGAAAGC	XP_016873780.1:n.4762+25_4762+26insACCATAGGCCTGAAAGC
XM_017018292.1:c.4144+25_4144+26insACCATAGGCCTGAAAGC	XP_016873781.1:n.4144+25_4144+26insACCATAGGCCTGAAAGC
XM_017018293.1:c.4762+25_4762+26insACCATAGGCCTGAAAGC	XP_016873782.1:n.4762+25_4762+26insACCATAGGCCTGAAAGC
NM_001377.3:c.4762+25_4762+26insACCATAGGCCTGAAAGC MANE Select	NP_001368.2:n.4762+25_4762+26insACCATAGGCCTGAAAGC
NM_001080463.2:c.4762+25_4762+26insACCATAGGCCTGAAAGC MANE Plus Clinical	NP_001073932.1:n.4762+25_4762+26insACCATAGGCCTGAAAGC