Canonical Allele Identifier: CA210505
Gene: DYNC2H1 HGNC NCBI

Linked Data

ClinVar Variation Id: 6506
dbSNP Id: rs137853030

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.103125197C>T , CM000673.2:g.103125197C>T GRCh38
NC_000011.9:g.102995926C>T , CM000673.1:g.102995926C>T GRCh37
NC_000011.8:g.102501136C>T NCBI36
NG_016423.1:g.20767C>T
NG_016423.2:g.20767C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650373.2:c.1759C>T MANE Plus Clinical ENSP00000497174.1:p.Arg587Cys
ENST00000375735.7:c.1759C>T MANE Select ENSP00000364887.2:p.Arg587Cys
ENST00000648198.1:c.1759C>T ENSP00000497329.1:p.Arg587Cys
ENST00000649323.1:c.1759C>T ENSP00000497581.1:p.Arg587Cys
ENST00000650373.1:c.1759C>T ENSP00000497174.1:p.Arg587Cys
ENST00000334267.11:c.1759C>T ENSP00000334021.7:p.Arg587Cys
ENST00000375735.6:c.1759C>T ENSP00000364887.2:p.Arg587Cys
ENST00000398093.7:c.1759C>T ENSP00000381167.3:p.Arg587Cys
NM_001080463.1:c.1759C>T NP_001073932.1:p.Arg587Cys
NM_001377.2:c.1759C>T NP_001368.2:p.Arg587Cys
XM_006718903.2:c.1759C>T XP_006718966.1:p.Arg587Cys
XM_017018291.1:c.1759C>T XP_016873780.1:p.Arg587Cys
XM_017018292.1:c.1141C>T XP_016873781.1:p.Arg381Cys
XM_017018293.1:c.1759C>T XP_016873782.1:p.Arg587Cys
NM_001377.3:c.1759C>T MANE Select NP_001368.2:p.Arg587Cys
NM_001080463.2:c.1759C>T MANE Plus Clinical NP_001073932.1:p.Arg587Cys