Canonical Allele Identifier: CA382239375

Gene: DYNC2H1

Linked Data

• gnomAD v4: 11-103165929-C-T
• MyVariant Identifiers: chr11:g.103036658C>T (hg19) ; chr11:g.103165929C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103165929C>T , CM000673.2:g.103165929C>T	GRCh38
NC_000011.9:g.103036658C>T , CM000673.1:g.103036658C>T	GRCh37
NC_000011.8:g.102541868C>T	NCBI36
NG_016423.1:g.61499C>T
NG_016423.2:g.61499C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.4643C>T MANE Plus Clinical	ENSP00000497174.1:p.Thr1548Ile
ENST00000375735.7:c.4643C>T MANE Select	ENSP00000364887.2:p.Thr1548Ile
ENST00000649323.1:c.*2188C>T	ENSP00000497581.1:n.*2188C>T
ENST00000650373.1:c.4643C>T	ENSP00000497174.1:p.Thr1548Ile
ENST00000334267.11:c.2205+31510C>T	ENSP00000334021.7:n.2205+31510C>T
ENST00000375735.6:c.4643C>T	ENSP00000364887.2:p.Thr1548Ile
ENST00000398093.7:c.4643C>T	ENSP00000381167.3:p.Thr1548Ile
NM_001080463.1:c.4643C>T	NP_001073932.1:p.Thr1548Ile
NM_001377.2:c.4643C>T	NP_001368.2:p.Thr1548Ile
XM_006718903.2:c.4643C>T	XP_006718966.1:p.Thr1548Ile
XM_017018291.1:c.4643C>T	XP_016873780.1:p.Thr1548Ile
XM_017018292.1:c.4025C>T	XP_016873781.1:p.Thr1342Ile
XM_017018293.1:c.4643C>T	XP_016873782.1:p.Thr1548Ile
NM_001377.3:c.4643C>T MANE Select	NP_001368.2:p.Thr1548Ile
NM_001080463.2:c.4643C>T MANE Plus Clinical	NP_001073932.1:p.Thr1548Ile