Canonical Allele Identifier: CA1996413682

Gene: DYNC2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103172992_103172994delinsTTA , CM000673.2:g.103172992_103172994delinsTTA	GRCh38
NC_000011.9:g.103043721_103043723delinsTTA , CM000673.1:g.103043721_103043723delinsTTA	GRCh37
NC_000011.8:g.102548931_102548933delinsTTA	NCBI36
NG_016423.1:g.68562_68564delinsTTA
NG_016423.2:g.68562_68564delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.5335-90_5335-88delinsTTA MANE Plus Clinical	ENSP00000497174.1:n.5335-90_5335-88delinsTTA
ENST00000375735.7:c.5335-90_5335-88delinsTTA MANE Select	ENSP00000364887.2:n.5335-90_5335-88delinsTTA
ENST00000649323.1:c.*2880-90_*2880-88delinsTTA	ENSP00000497581.1:n.*2880-90_*2880-88delinsTTA
ENST00000650373.1:c.5335-90_5335-88delinsTTA	ENSP00000497174.1:n.5335-90_5335-88delinsTTA
ENST00000334267.11:c.2205+38573_2205+38575delinsTTA	ENSP00000334021.7:n.2205+38573_2205+38575delinsTTA
ENST00000375735.6:c.5335-90_5335-88delinsTTA	ENSP00000364887.2:n.5335-90_5335-88delinsTTA
ENST00000398093.7:c.5335-90_5335-88delinsTTA	ENSP00000381167.3:n.5335-90_5335-88delinsTTA
NM_001080463.1:c.5335-90_5335-88delinsTTA	NP_001073932.1:n.5335-90_5335-88delinsTTA
NM_001377.2:c.5335-90_5335-88delinsTTA	NP_001368.2:n.5335-90_5335-88delinsTTA
XM_006718903.2:c.5335-90_5335-88delinsTTA	XP_006718966.1:n.5335-90_5335-88delinsTTA
XM_017018291.1:c.5335-90_5335-88delinsTTA	XP_016873780.1:n.5335-90_5335-88delinsTTA
XM_017018292.1:c.4717-90_4717-88delinsTTA	XP_016873781.1:n.4717-90_4717-88delinsTTA
XM_017018293.1:c.5335-90_5335-88delinsTTA	XP_016873782.1:n.5335-90_5335-88delinsTTA
NM_001377.3:c.5335-90_5335-88delinsTTA MANE Select	NP_001368.2:n.5335-90_5335-88delinsTTA
NM_001080463.2:c.5335-90_5335-88delinsTTA MANE Plus Clinical	NP_001073932.1:n.5335-90_5335-88delinsTTA