Canonical Allele Identifier: CA382262667

Gene: DYNC2H1

Linked Data

• MyVariant Identifiers: chr11:g.103091362A>C (hg19) ; chr11:g.103220633A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103220633A>C , CM000673.2:g.103220633A>C	GRCh38
NC_000011.9:g.103091362A>C , CM000673.1:g.103091362A>C	GRCh37
NC_000011.8:g.102596572A>C	NCBI36
NG_016423.1:g.116203A>C
NG_016423.2:g.116203A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.8957A>C MANE Plus Clinical	ENSP00000497174.1:p.Asn2986Thr
ENST00000375735.7:c.8957A>C MANE Select	ENSP00000364887.2:p.Asn2986Thr
ENST00000650373.1:c.8957A>C	ENSP00000497174.1:p.Asn2986Thr
ENST00000334267.11:c.2205+86214A>C	ENSP00000334021.7:n.2205+86214A>C
ENST00000375735.6:c.8957A>C	ENSP00000364887.2:p.Asn2986Thr
ENST00000398093.7:c.8957A>C	ENSP00000381167.3:p.Asn2986Thr
NM_001080463.1:c.8957A>C	NP_001073932.1:p.Asn2986Thr
NM_001377.2:c.8957A>C	NP_001368.2:p.Asn2986Thr
XM_006718903.2:c.8936A>C	XP_006718966.1:p.Asn2979Thr
XM_017018291.1:c.8957A>C	XP_016873780.1:p.Asn2986Thr
XM_017018292.1:c.8339A>C	XP_016873781.1:p.Asn2780Thr
NM_001377.3:c.8957A>C MANE Select	NP_001368.2:p.Asn2986Thr
NM_001080463.2:c.8957A>C MANE Plus Clinical	NP_001073932.1:p.Asn2986Thr