Canonical Allele Identifier: CA16427940
Gene: DYNC2H1 HGNC NCBI

Linked Data

dbSNP Id: rs11225703

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.103315230C>T , CM000673.2:g.103315230C>T GRCh38
NC_000011.9:g.103185959C>T , CM000673.1:g.103185959C>T GRCh37
NC_000011.8:g.102691169C>T NCBI36
NG_016423.1:g.210800C>T
NG_016423.2:g.210800C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650373.2:c.11671-1315C>T MANE Plus Clinical ENSP00000497174.1:n.11671-1315C>T
ENST00000375735.7:c.11650-1315C>T MANE Select ENSP00000364887.2:n.11650-1315C>T
ENST00000650373.1:c.11671-1315C>T ENSP00000497174.1:n.11671-1315C>T
ENST00000334267.11:c.2206-120713C>T ENSP00000334021.7:n.2206-120713C>T
ENST00000375735.6:c.11650-1315C>T ENSP00000364887.2:n.11650-1315C>T
ENST00000398093.7:c.11671-1315C>T ENSP00000381167.3:n.11671-1315C>T
ENST00000528670.5:c.829-1315C>T ENSP00000433451.1:n.829-1315C>T
NM_001080463.1:c.11671-1315C>T NP_001073932.1:n.11671-1315C>T
NM_001377.2:c.11650-1315C>T NP_001368.2:n.11650-1315C>T
XM_006718903.2:c.11629-1315C>T XP_006718966.1:n.11629-1315C>T
XM_017018291.1:c.11650-1315C>T XP_016873780.1:n.11650-1315C>T
XM_017018292.1:c.11032-1315C>T XP_016873781.1:n.11032-1315C>T
NM_001377.3:c.11650-1315C>T MANE Select NP_001368.2:n.11650-1315C>T
NM_001080463.2:c.11671-1315C>T MANE Plus Clinical NP_001073932.1:n.11671-1315C>T