Canonical Allele Identifier: CA382239306
Gene: DYNC2H1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.103165900T>G , CM000673.2:g.103165900T>G GRCh38
NC_000011.9:g.103036629T>G , CM000673.1:g.103036629T>G GRCh37
NC_000011.8:g.102541839T>G NCBI36
NG_016423.1:g.61470T>G
NG_016423.2:g.61470T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650373.2:c.4614T>G MANE Plus Clinical ENSP00000497174.1:p.Ile1538Met
ENST00000375735.7:c.4614T>G MANE Select ENSP00000364887.2:p.Ile1538Met
ENST00000649323.1:c.*2159T>G ENSP00000497581.1:n.*2159T>G
ENST00000650373.1:c.4614T>G ENSP00000497174.1:p.Ile1538Met
ENST00000334267.11:c.2205+31481T>G ENSP00000334021.7:n.2205+31481T>G
ENST00000375735.6:c.4614T>G ENSP00000364887.2:p.Ile1538Met
ENST00000398093.7:c.4614T>G ENSP00000381167.3:p.Ile1538Met
NM_001080463.1:c.4614T>G NP_001073932.1:p.Ile1538Met
NM_001377.2:c.4614T>G NP_001368.2:p.Ile1538Met
XM_006718903.2:c.4614T>G XP_006718966.1:p.Ile1538Met
XM_017018291.1:c.4614T>G XP_016873780.1:p.Ile1538Met
XM_017018292.1:c.3996T>G XP_016873781.1:p.Ile1332Met
XM_017018293.1:c.4614T>G XP_016873782.1:p.Ile1538Met
NM_001377.3:c.4614T>G MANE Select NP_001368.2:p.Ile1538Met
NM_001080463.2:c.4614T>G MANE Plus Clinical NP_001073932.1:p.Ile1538Met