Canonical Allele Identifier: CA1996392170

Gene: DYNC2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103125281_103125287delinsATTATTC , CM000673.2:g.103125281_103125287delinsATTATTC	GRCh38
NC_000011.9:g.102996010_102996016delinsATTATTC , CM000673.1:g.102996010_102996016delinsATTATTC	GRCh37
NC_000011.8:g.102501220_102501226delinsATTATTC	NCBI36
NG_016423.1:g.20851_20857delinsATTATTC
NG_016423.2:g.20851_20857delinsATTATTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.1843_1849delinsATTATTC MANE Plus Clinical	ENSP00000497174.1:p.Ile615=
ENST00000375735.7:c.1843_1849delinsATTATTC MANE Select	ENSP00000364887.2:p.Ile615=
ENST00000648198.1:c.1843_1849delinsATTATTC	ENSP00000497329.1:p.Ile615=
ENST00000649323.1:c.1843_1849delinsATTATTC	ENSP00000497581.1:p.Ile615=
ENST00000650373.1:c.1843_1849delinsATTATTC	ENSP00000497174.1:p.Ile615=
ENST00000334267.11:c.1843_1849delinsATTATTC	ENSP00000334021.7:p.Ile615=
ENST00000375735.6:c.1843_1849delinsATTATTC	ENSP00000364887.2:p.Ile615=
ENST00000398093.7:c.1843_1849delinsATTATTC	ENSP00000381167.3:p.Ile615=
NM_001080463.1:c.1843_1849delinsATTATTC	NP_001073932.1:p.Ile615=
NM_001377.2:c.1843_1849delinsATTATTC	NP_001368.2:p.Ile615=
XM_006718903.2:c.1843_1849delinsATTATTC	XP_006718966.1:p.Ile615=
XM_017018291.1:c.1843_1849delinsATTATTC	XP_016873780.1:p.Ile615=
XM_017018292.1:c.1225_1231delinsATTATTC	XP_016873781.1:p.Ile409=
XM_017018293.1:c.1843_1849delinsATTATTC	XP_016873782.1:p.Ile615=
NM_001377.3:c.1843_1849delinsATTATTC MANE Select	NP_001368.2:p.Ile615=
NM_001080463.2:c.1843_1849delinsATTATTC MANE Plus Clinical	NP_001073932.1:p.Ile615=