Canonical Allele Identifier: CA2615751337

Gene: DYNC2H1

Linked Data

• gnomAD v4: 11-103256362-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103256362A>T , CM000673.2:g.103256362A>T	GRCh38
NC_000011.9:g.103127091A>T , CM000673.1:g.103127091A>T	GRCh37
NC_000011.8:g.102632301A>T	NCBI36
NG_016423.1:g.151932A>T
NG_016423.2:g.151932A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650373.2:c.10482+122A>T MANE Plus Clinical	ENSP00000497174.1:n.10482+122A>T
ENST00000375735.7:c.10461+122A>T MANE Select	ENSP00000364887.2:n.10461+122A>T
ENST00000650373.1:c.10482+122A>T	ENSP00000497174.1:n.10482+122A>T
ENST00000334267.11:c.2205+121943A>T	ENSP00000334021.7:n.2205+121943A>T
ENST00000375735.6:c.10461+122A>T	ENSP00000364887.2:n.10461+122A>T
ENST00000398093.7:c.10482+122A>T	ENSP00000381167.3:n.10482+122A>T
NM_001080463.1:c.10482+122A>T	NP_001073932.1:n.10482+122A>T
NM_001377.2:c.10461+122A>T	NP_001368.2:n.10461+122A>T
XM_006718903.2:c.10440+122A>T	XP_006718966.1:n.10440+122A>T
XM_017018291.1:c.10461+122A>T	XP_016873780.1:n.10461+122A>T
XM_017018292.1:c.9843+122A>T	XP_016873781.1:n.9843+122A>T
NM_001377.3:c.10461+122A>T MANE Select	NP_001368.2:n.10461+122A>T
NM_001080463.2:c.10482+122A>T MANE Plus Clinical	NP_001073932.1:n.10482+122A>T