Canonical Allele Identifier: CA1996390398
Gene: DYNC2H1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.103121070_103121073delinsGAGA , CM000673.2:g.103121070_103121073delinsGAGA GRCh38
NC_000011.9:g.102991799_102991802delinsGAGA , CM000673.1:g.102991799_102991802delinsGAGA GRCh37
NC_000011.8:g.102497009_102497012delinsGAGA NCBI36
NG_016423.1:g.16640_16643delinsGAGA
NG_016423.2:g.16640_16643delinsGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650373.2:c.1360+34_1360+37delinsGAGA MANE Plus Clinical ENSP00000497174.1:n.1360+34_1360+37delinsGAGA
ENST00000375735.7:c.1360+34_1360+37delinsGAGA MANE Select ENSP00000364887.2:n.1360+34_1360+37delinsGAGA
ENST00000648198.1:c.1360+34_1360+37delinsGAGA ENSP00000497329.1:n.1360+34_1360+37delinsGAGA
ENST00000649323.1:c.1360+34_1360+37delinsGAGA ENSP00000497581.1:n.1360+34_1360+37delinsGAGA
ENST00000650373.1:c.1360+34_1360+37delinsGAGA ENSP00000497174.1:n.1360+34_1360+37delinsGAGA
ENST00000334267.11:c.1360+34_1360+37delinsGAGA ENSP00000334021.7:n.1360+34_1360+37delinsGAGA
ENST00000375735.6:c.1360+34_1360+37delinsGAGA ENSP00000364887.2:n.1360+34_1360+37delinsGAGA
ENST00000398093.7:c.1360+34_1360+37delinsGAGA ENSP00000381167.3:n.1360+34_1360+37delinsGAGA
NM_001080463.1:c.1360+34_1360+37delinsGAGA NP_001073932.1:n.1360+34_1360+37delinsGAGA
NM_001377.2:c.1360+34_1360+37delinsGAGA NP_001368.2:n.1360+34_1360+37delinsGAGA
XM_006718903.2:c.1360+34_1360+37delinsGAGA XP_006718966.1:n.1360+34_1360+37delinsGAGA
XM_017018291.1:c.1360+34_1360+37delinsGAGA XP_016873780.1:n.1360+34_1360+37delinsGAGA
XM_017018292.1:c.742+34_742+37delinsGAGA XP_016873781.1:n.742+34_742+37delinsGAGA
XM_017018293.1:c.1360+34_1360+37delinsGAGA XP_016873782.1:n.1360+34_1360+37delinsGAGA
NM_001377.3:c.1360+34_1360+37delinsGAGA MANE Select NP_001368.2:n.1360+34_1360+37delinsGAGA
NM_001080463.2:c.1360+34_1360+37delinsGAGA MANE Plus Clinical NP_001073932.1:n.1360+34_1360+37delinsGAGA