Canonical Allele Identifier: CA155058092

Gene: DNAH11

Linked Data

• dbSNP Id: rs1026737742
• gnomAD v3: 7-21567711-G-A
• gnomAD v4: 7-21567711-G-A
• MyVariant Identifiers: chr7:g.21607329G>A (hg19) ; chr7:g.21567711G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21567711G>A , CM000669.2:g.21567711G>A	GRCh38
NC_000007.13:g.21607329G>A , CM000669.1:g.21607329G>A	GRCh37
NC_000007.12:g.21573854G>A	NCBI36
NG_012886.2:g.29497G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.1195-2358G>A MANE Select	ENSP00000475939.1:n.1195-2358G>A
ENST00000328843.10:c.1195-2358G>A	ENSP00000330671.7:n.1195-2358G>A
ENST00000409508.7:c.1195-2358G>A	ENSP00000475939.1:n.1195-2358G>A
ENST00000496218.1:n.81-2358G>A
ENST00000620169.4:c.1195-2358G>A	ENSP00000481693.1:n.1195-2358G>A
NM_001277115.1:c.1195-2358G>A	NP_001264044.1:n.1195-2358G>A
XR_927090.1:n.563+5615C>T
XR_001745114.1:n.2793+5615C>T
NM_001277115.2:c.1195-2358G>A MANE Select	NP_001264044.1:n.1195-2358G>A