Canonical Allele Identifier: CA601669965

Gene: DYNC2H1

Linked Data

• dbSNP Id: rs1565315620
• gnomAD v2: 11-102991815-ATTAC-A
• gnomAD v4: 11-103121086-ATTAC-A
• MyVariant Identifiers: chr11:g.102991816_102991819del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103121089_103121092del , CM000673.2:g.103121089_103121092del	GRCh38
NC_000011.9:g.102991818_102991821del , CM000673.1:g.102991818_102991821del	GRCh37
NC_000011.8:g.102497028_102497031del	NCBI36
NG_016423.1:g.16659_16662del
NG_016423.2:g.16659_16662del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.1360+53_1360+56del MANE Plus Clinical	ENSP00000497174.1:n.1360+53_1360+56del
ENST00000375735.7:c.1360+53_1360+56del MANE Select	ENSP00000364887.2:n.1360+53_1360+56del
ENST00000648198.1:c.1360+53_1360+56del	ENSP00000497329.1:n.1360+53_1360+56del
ENST00000649323.1:c.1360+53_1360+56del	ENSP00000497581.1:n.1360+53_1360+56del
ENST00000650373.1:c.1360+53_1360+56del	ENSP00000497174.1:n.1360+53_1360+56del
ENST00000334267.11:c.1360+53_1360+56del	ENSP00000334021.7:n.1360+53_1360+56del
ENST00000375735.6:c.1360+53_1360+56del	ENSP00000364887.2:n.1360+53_1360+56del
ENST00000398093.7:c.1360+53_1360+56del	ENSP00000381167.3:n.1360+53_1360+56del
NM_001080463.1:c.1360+53_1360+56del	NP_001073932.1:n.1360+53_1360+56del
NM_001377.2:c.1360+53_1360+56del	NP_001368.2:n.1360+53_1360+56del
XM_006718903.2:c.1360+53_1360+56del	XP_006718966.1:n.1360+53_1360+56del
XM_017018291.1:c.1360+53_1360+56del	XP_016873780.1:n.1360+53_1360+56del
XM_017018292.1:c.742+53_742+56del	XP_016873781.1:n.742+53_742+56del
XM_017018293.1:c.1360+53_1360+56del	XP_016873782.1:n.1360+53_1360+56del
NM_001377.3:c.1360+53_1360+56del MANE Select	NP_001368.2:n.1360+53_1360+56del
NM_001080463.2:c.1360+53_1360+56del MANE Plus Clinical	NP_001073932.1:n.1360+53_1360+56del