Canonical Allele Identifier: CA6254727

Gene: DYNC2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103235659C>G , CM000673.2:g.103235659C>G	GRCh38
NC_000011.9:g.103106388C>G , CM000673.1:g.103106388C>G	GRCh37
NC_000011.8:g.102611598C>G	NCBI36
NG_016423.1:g.131229C>G
NG_016423.2:g.131229C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001377.3:c.9568-13C>G MANE Select	NP_001368.2:n.9568-13C>G
ENST00000375735.7:c.9568-13C>G MANE Select	ENSP00000364887.2:n.9568-13C>G
NM_001080463.2:c.9568-13C>G MANE Plus Clinical	NP_001073932.1:n.9568-13C>G
ENST00000650373.2:c.9568-13C>G MANE Plus Clinical	ENSP00000497174.1:n.9568-13C>G
NM_001080463.1:c.9568-13C>G	NP_001073932.1:n.9568-13C>G
NM_001377.2:c.9568-13C>G	NP_001368.2:n.9568-13C>G
ENST00000334267.11:c.2205+101240C>G	ENSP00000334021.7:n.2205+101240C>G
ENST00000375735.6:c.9568-13C>G	ENSP00000364887.2:n.9568-13C>G
ENST00000398093.7:c.9568-13C>G	ENSP00000381167.3:n.9568-13C>G
ENST00000650373.1:c.9568-13C>G	ENSP00000497174.1:n.9568-13C>G
XM_006718903.2:c.9547-13C>G	XP_006718966.1:n.9547-13C>G
XM_017018291.1:c.9568-13C>G	XP_016873780.1:n.9568-13C>G
XM_017018292.1:c.8950-13C>G	XP_016873781.1:n.8950-13C>G