Canonical Allele Identifier: CA1099232983

Gene: DNAH11

Linked Data

• dbSNP Id: rs1783192773
• gnomAD v3: 7-21864469-A-T
• gnomAD v4: 7-21864469-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21864469A>T , CM000669.2:g.21864469A>T	GRCh38
NC_000007.13:g.21904087A>T , CM000669.1:g.21904087A>T	GRCh37
NC_000007.12:g.21870612A>T	NCBI36
NG_012886.2:g.326255A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.11374-66A>T MANE Select	ENSP00000475939.1:n.11374-66A>T
ENST00000328843.10:c.11395-66A>T	ENSP00000330671.7:n.11395-66A>T
ENST00000409508.7:c.11374-66A>T	ENSP00000475939.1:n.11374-66A>T
ENST00000620169.4:c.11395-66A>T	ENSP00000481693.1:n.11395-66A>T
NM_001277115.1:c.11374-66A>T	NP_001264044.1:n.11374-66A>T
NM_001277115.2:c.11374-66A>T MANE Select	NP_001264044.1:n.11374-66A>T