Canonical Allele Identifier: CA382262882

Gene: DYNC2H1

Linked Data

• MyVariant Identifiers: chr11:g.103091463G>T (hg19) ; chr11:g.103220734G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103220734G>T , CM000673.2:g.103220734G>T	GRCh38
NC_000011.9:g.103091463G>T , CM000673.1:g.103091463G>T	GRCh37
NC_000011.8:g.102596673G>T	NCBI36
NG_016423.1:g.116304G>T
NG_016423.2:g.116304G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.9058G>T MANE Plus Clinical	ENSP00000497174.1:p.Val3020Phe
ENST00000375735.7:c.9058G>T MANE Select	ENSP00000364887.2:p.Val3020Phe
ENST00000650373.1:c.9058G>T	ENSP00000497174.1:p.Val3020Phe
ENST00000334267.11:c.2205+86315G>T	ENSP00000334021.7:n.2205+86315G>T
ENST00000375735.6:c.9058G>T	ENSP00000364887.2:p.Val3020Phe
ENST00000398093.7:c.9058G>T	ENSP00000381167.3:p.Val3020Phe
NM_001080463.1:c.9058G>T	NP_001073932.1:p.Val3020Phe
NM_001377.2:c.9058G>T	NP_001368.2:p.Val3020Phe
XM_006718903.2:c.9037G>T	XP_006718966.1:p.Val3013Phe
XM_017018291.1:c.9058G>T	XP_016873780.1:p.Val3020Phe
XM_017018292.1:c.8440G>T	XP_016873781.1:p.Val2814Phe
NM_001377.3:c.9058G>T MANE Select	NP_001368.2:p.Val3020Phe
NM_001080463.2:c.9058G>T MANE Plus Clinical	NP_001073932.1:p.Val3020Phe