Canonical Allele Identifier: CA2724810056

Gene: DYNC2H1

Linked Data

• dbSNP Id: rs2134945590

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103166136dup , CM000673.2:g.103166136dup	GRCh38
NC_000011.9:g.103036865dup , CM000673.1:g.103036865dup	GRCh37
NC_000011.8:g.102542075dup	NCBI36
NG_016423.1:g.61706dup
NG_016423.2:g.61706dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.4762+88dup MANE Plus Clinical	ENSP00000497174.1:n.4762+88dup
ENST00000375735.7:c.4762+88dup MANE Select	ENSP00000364887.2:n.4762+88dup
ENST00000649323.1:c.*2307+88dup	ENSP00000497581.1:n.*2307+88dup
ENST00000650373.1:c.4762+88dup	ENSP00000497174.1:n.4762+88dup
ENST00000334267.11:c.2205+31717dup	ENSP00000334021.7:n.2205+31717dup
ENST00000375735.6:c.4762+88dup	ENSP00000364887.2:n.4762+88dup
ENST00000398093.7:c.4762+88dup	ENSP00000381167.3:n.4762+88dup
NM_001080463.1:c.4762+88dup	NP_001073932.1:n.4762+88dup
NM_001377.2:c.4762+88dup	NP_001368.2:n.4762+88dup
XM_006718903.2:c.4762+88dup	XP_006718966.1:n.4762+88dup
XM_017018291.1:c.4762+88dup	XP_016873780.1:n.4762+88dup
XM_017018292.1:c.4144+88dup	XP_016873781.1:n.4144+88dup
XM_017018293.1:c.4762+88dup	XP_016873782.1:n.4762+88dup
NM_001377.3:c.4762+88dup MANE Select	NP_001368.2:n.4762+88dup
NM_001080463.2:c.4762+88dup MANE Plus Clinical	NP_001073932.1:n.4762+88dup