Canonical Allele Identifier: CA353115381

Gene: DNAH1

Linked Data

• gnomAD v4: 3-52353601-G-T
• MyVariant Identifiers: chr3:g.52387617G>T (hg19) ; chr3:g.52353601G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52353601G>T , CM000665.2:g.52353601G>T	GRCh38
NC_000003.11:g.52387617G>T , CM000665.1:g.52387617G>T	GRCh37
NC_000003.10:g.52362657G>T	NCBI36
NG_052911.1:g.42283G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420323.7:c.3448G>T MANE Select	ENSP00000401514.2:p.Glu1150Ter
ENST00000420323.6:c.3448G>T	ENSP00000401514.2:p.Glu1150Ter
ENST00000486752.5:n.3709G>T
ENST00000497875.1:n.3613G>T
NM_015512.4:c.3448G>T	NP_056327.4:p.Glu1150Ter
XM_011533577.1:c.3448G>T	XP_011531879.1:p.Glu1150Ter
XM_017006129.1:c.3448G>T	XP_016861618.1:p.Glu1150Ter
XM_017006130.1:c.3448G>T	XP_016861619.1:p.Glu1150Ter
XM_017006131.1:c.3448G>T	XP_016861620.1:p.Glu1150Ter
XM_017006132.1:c.3448G>T	XP_016861621.1:p.Glu1150Ter
XM_017006133.1:c.3448G>T	XP_016861622.1:p.Glu1150Ter
XR_001740098.1:n.6597G>T
XR_001740099.1:n.6597G>T
NM_015512.5:c.3448G>T MANE Select	NP_056327.4:p.Glu1150Ter