Canonical Allele Identifier: CA6255685

Gene: DYNC2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103479088dup , CM000673.2:g.103479088dup	GRCh38
NC_000011.9:g.103349816dup , CM000673.1:g.103349816dup	GRCh37
NC_000011.8:g.102855026dup	NCBI36
NG_016423.1:g.374657dup
NG_016423.2:g.374658dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001377.3:c.12766-7dup MANE Select	NP_001368.2:n.12766-7dup
ENST00000375735.7:c.12766-7dup MANE Select	ENSP00000364887.2:n.12766-7dup
NM_001080463.2:c.12787-7dup MANE Plus Clinical	NP_001073932.1:n.12787-7dup
ENST00000650373.2:c.12787-7dup MANE Plus Clinical	ENSP00000497174.1:n.12787-7dup
NM_001080463.1:c.12787-7dup	NP_001073932.1:n.12787-7dup
NM_001377.2:c.12766-7dup	NP_001368.2:n.12766-7dup
ENST00000334267.11:c.2605-7dup	ENSP00000334021.7:n.2605-7dup
ENST00000375735.6:c.12766-7dup	ENSP00000364887.2:n.12766-7dup
ENST00000398093.7:c.12787-7dup	ENSP00000381167.3:n.12787-7dup
ENST00000527252.1:n.318-7dup
ENST00000528670.5:c.1949-7dup	ENSP00000433451.1:n.1949-7dup
ENST00000530547.1:n.497-7dup
ENST00000533197.1:c.517-7dup	ENSP00000436736.1:n.517-7dup
ENST00000650373.1:c.12787-7dup	ENSP00000497174.1:n.12787-7dup
XM_006718903.2:c.12745-7dup	XP_006718966.1:n.12745-7dup
XM_017018291.1:c.12556-7dup	XP_016873780.1:n.12556-7dup
XM_017018292.1:c.12148-7dup	XP_016873781.1:n.12148-7dup