Canonical Allele Identifier: CA1996449667

Gene: DYNC2H1

Linked Data

• dbSNP Id: rs1865061153

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103256455del , CM000673.2:g.103256455del	GRCh38
NC_000011.9:g.103127184del , CM000673.1:g.103127184del	GRCh37
NC_000011.8:g.102632394del	NCBI36
NG_016423.1:g.152025del
NG_016423.2:g.152025del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.10482+215del MANE Plus Clinical	ENSP00000497174.1:n.10482+215del
ENST00000375735.7:c.10461+215del MANE Select	ENSP00000364887.2:n.10461+215del
ENST00000650373.1:c.10482+215del	ENSP00000497174.1:n.10482+215del
ENST00000334267.11:c.2205+122036del	ENSP00000334021.7:n.2205+122036del
ENST00000375735.6:c.10461+215del	ENSP00000364887.2:n.10461+215del
ENST00000398093.7:c.10482+215del	ENSP00000381167.3:n.10482+215del
NM_001080463.1:c.10482+215del	NP_001073932.1:n.10482+215del
NM_001377.2:c.10461+215del	NP_001368.2:n.10461+215del
XM_006718903.2:c.10440+215del	XP_006718966.1:n.10440+215del
XM_017018291.1:c.10461+215del	XP_016873780.1:n.10461+215del
XM_017018292.1:c.9843+215del	XP_016873781.1:n.9843+215del
NM_001377.3:c.10461+215del MANE Select	NP_001368.2:n.10461+215del
NM_001080463.2:c.10482+215del MANE Plus Clinical	NP_001073932.1:n.10482+215del