Canonical Allele Identifier: CA227395987
Gene: DYNC2H1 HGNC NCBI

Linked Data

dbSNP Id: rs1040540931

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.103165840A>C , CM000673.2:g.103165840A>C GRCh38
NC_000011.9:g.103036569A>C , CM000673.1:g.103036569A>C GRCh37
NC_000011.8:g.102541779A>C NCBI36
NG_016423.1:g.61410A>C
NG_016423.2:g.61410A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650373.2:c.4612-58A>C MANE Plus Clinical ENSP00000497174.1:n.4612-58A>C
ENST00000375735.7:c.4612-58A>C MANE Select ENSP00000364887.2:n.4612-58A>C
ENST00000649323.1:c.*2157-58A>C ENSP00000497581.1:n.*2157-58A>C
ENST00000650373.1:c.4612-58A>C ENSP00000497174.1:n.4612-58A>C
ENST00000334267.11:c.2205+31421A>C ENSP00000334021.7:n.2205+31421A>C
ENST00000375735.6:c.4612-58A>C ENSP00000364887.2:n.4612-58A>C
ENST00000398093.7:c.4612-58A>C ENSP00000381167.3:n.4612-58A>C
NM_001080463.1:c.4612-58A>C NP_001073932.1:n.4612-58A>C
NM_001377.2:c.4612-58A>C NP_001368.2:n.4612-58A>C
XM_006718903.2:c.4612-58A>C XP_006718966.1:n.4612-58A>C
XM_017018291.1:c.4612-58A>C XP_016873780.1:n.4612-58A>C
XM_017018292.1:c.3994-58A>C XP_016873781.1:n.3994-58A>C
XM_017018293.1:c.4612-58A>C XP_016873782.1:n.4612-58A>C
NM_001377.3:c.4612-58A>C MANE Select NP_001368.2:n.4612-58A>C
NM_001080463.2:c.4612-58A>C MANE Plus Clinical NP_001073932.1:n.4612-58A>C