Canonical Allele Identifier: CA2681990788

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21854278-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21854278G>C , CM000669.2:g.21854278G>C	GRCh38
NC_000007.13:g.21893896G>C , CM000669.1:g.21893896G>C	GRCh37
NC_000007.12:g.21860421G>C	NCBI36
NG_012886.2:g.316064G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.11062-37G>C MANE Select	ENSP00000475939.1:n.11062-37G>C
ENST00000328843.10:c.11083-37G>C	ENSP00000330671.7:n.11083-37G>C
ENST00000409508.7:c.11062-37G>C	ENSP00000475939.1:n.11062-37G>C
ENST00000421290.1:n.245-37G>C
ENST00000607413.5:n.325-37G>C
ENST00000620169.4:c.11083-37G>C	ENSP00000481693.1:n.11083-37G>C
NM_001277115.1:c.11062-37G>C	NP_001264044.1:n.11062-37G>C
NM_001277115.2:c.11062-37G>C MANE Select	NP_001264044.1:n.11062-37G>C