Canonical Allele Identifier: CA382255136
Gene: DYNC2H1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.103125228C>G , CM000673.2:g.103125228C>G GRCh38
NC_000011.9:g.102995957C>G , CM000673.1:g.102995957C>G GRCh37
NC_000011.8:g.102501167C>G NCBI36
NG_016423.1:g.20798C>G
NG_016423.2:g.20798C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650373.2:c.1790C>G MANE Plus Clinical ENSP00000497174.1:p.Pro597Arg
ENST00000375735.7:c.1790C>G MANE Select ENSP00000364887.2:p.Pro597Arg
ENST00000648198.1:c.1790C>G ENSP00000497329.1:p.Pro597Arg
ENST00000649323.1:c.1790C>G ENSP00000497581.1:p.Pro597Arg
ENST00000650373.1:c.1790C>G ENSP00000497174.1:p.Pro597Arg
ENST00000334267.11:c.1790C>G ENSP00000334021.7:p.Pro597Arg
ENST00000375735.6:c.1790C>G ENSP00000364887.2:p.Pro597Arg
ENST00000398093.7:c.1790C>G ENSP00000381167.3:p.Pro597Arg
NM_001080463.1:c.1790C>G NP_001073932.1:p.Pro597Arg
NM_001377.2:c.1790C>G NP_001368.2:p.Pro597Arg
XM_006718903.2:c.1790C>G XP_006718966.1:p.Pro597Arg
XM_017018291.1:c.1790C>G XP_016873780.1:p.Pro597Arg
XM_017018292.1:c.1172C>G XP_016873781.1:p.Pro391Arg
XM_017018293.1:c.1790C>G XP_016873782.1:p.Pro597Arg
NM_001377.3:c.1790C>G MANE Select NP_001368.2:p.Pro597Arg
NM_001080463.2:c.1790C>G MANE Plus Clinical NP_001073932.1:p.Pro597Arg