Canonical Allele Identifier: CA1099217244

Gene: DNAH11

Linked Data

• dbSNP Id: rs1786277226
• gnomAD v4: 7-21748849-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21748849T>C , CM000669.2:g.21748849T>C	GRCh38
NC_000007.13:g.21788467T>C , CM000669.1:g.21788467T>C	GRCh37
NC_000007.12:g.21754992T>C	NCBI36
NG_012886.2:g.210635T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.8673+107T>C MANE Select	ENSP00000475939.1:n.8673+107T>C
ENST00000328843.10:c.8694+107T>C	ENSP00000330671.7:n.8694+107T>C
ENST00000409508.7:c.8673+107T>C	ENSP00000475939.1:n.8673+107T>C
ENST00000620169.4:c.8694+107T>C	ENSP00000481693.1:n.8694+107T>C
NM_001277115.1:c.8673+107T>C	NP_001264044.1:n.8673+107T>C
NM_001277115.2:c.8673+107T>C MANE Select	NP_001264044.1:n.8673+107T>C