Canonical Allele Identifier: CA2615740972

Gene: DYNC2H1

Linked Data

• gnomAD v4: 11-103120899-CATGTACTTATTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103120900_103120911del , CM000673.2:g.103120900_103120911del	GRCh38
NC_000011.9:g.102991629_102991640del , CM000673.1:g.102991629_102991640del	GRCh37
NC_000011.8:g.102496839_102496850del	NCBI36
NG_016423.1:g.16470_16481del
NG_016423.2:g.16470_16481del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650373.2:c.1249-25_1249-14del MANE Plus Clinical	ENSP00000497174.1:n.1249-25_1249-14del
ENST00000375735.7:c.1249-25_1249-14del MANE Select	ENSP00000364887.2:n.1249-25_1249-14del
ENST00000648198.1:c.1249-25_1249-14del	ENSP00000497329.1:n.1249-25_1249-14del
ENST00000649323.1:c.1249-25_1249-14del	ENSP00000497581.1:n.1249-25_1249-14del
ENST00000650373.1:c.1249-25_1249-14del	ENSP00000497174.1:n.1249-25_1249-14del
ENST00000334267.11:c.1249-25_1249-14del	ENSP00000334021.7:n.1249-25_1249-14del
ENST00000375735.6:c.1249-25_1249-14del	ENSP00000364887.2:n.1249-25_1249-14del
ENST00000398093.7:c.1249-25_1249-14del	ENSP00000381167.3:n.1249-25_1249-14del
NM_001080463.1:c.1249-25_1249-14del	NP_001073932.1:n.1249-25_1249-14del
NM_001377.2:c.1249-25_1249-14del	NP_001368.2:n.1249-25_1249-14del
XM_006718903.2:c.1249-25_1249-14del	XP_006718966.1:n.1249-25_1249-14del
XM_017018291.1:c.1249-25_1249-14del	XP_016873780.1:n.1249-25_1249-14del
XM_017018292.1:c.631-25_631-14del	XP_016873781.1:n.631-25_631-14del
XM_017018293.1:c.1249-25_1249-14del	XP_016873782.1:n.1249-25_1249-14del
NM_001377.3:c.1249-25_1249-14del MANE Select	NP_001368.2:n.1249-25_1249-14del
NM_001080463.2:c.1249-25_1249-14del MANE Plus Clinical	NP_001073932.1:n.1249-25_1249-14del