Canonical Allele Identifier: CA2615741169

Gene: DYNC2H1

Linked Data

• gnomAD v4: 11-103121038-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103121042del , CM000673.2:g.103121042del	GRCh38
NC_000011.9:g.102991771del , CM000673.1:g.102991771del	GRCh37
NC_000011.8:g.102496981del	NCBI36
NG_016423.1:g.16612del
NG_016423.2:g.16612del

Transcript Alleles

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