Canonical Allele Identifier: CA4180015

Gene: DNAH11

Linked Data

• dbSNP Id: rs762149168
• ExAC: 7:21658861 T / C
• gnomAD v2: 7-21658861-T-C
• gnomAD v4: 7-21619243-T-C
• MyVariant Identifiers: chr7:g.21658861T>C (hg19) ; chr7:g.21619243T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21619243T>C , CM000669.2:g.21619243T>C	GRCh38
NC_000007.13:g.21658861T>C , CM000669.1:g.21658861T>C	GRCh37
NC_000007.12:g.21625386T>C	NCBI36
NG_012886.2:g.81029T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.4377+21T>C MANE Select	ENSP00000475939.1:n.4377+21T>C
ENST00000328843.10:c.4392+21T>C	ENSP00000330671.7:n.4392+21T>C
ENST00000409508.7:c.4377+21T>C	ENSP00000475939.1:n.4377+21T>C
ENST00000465593.1:n.403+21T>C
ENST00000620169.4:c.4392+21T>C	ENSP00000481693.1:n.4392+21T>C
NM_001277115.1:c.4377+21T>C	NP_001264044.1:n.4377+21T>C
NM_001277115.2:c.4377+21T>C MANE Select	NP_001264044.1:n.4377+21T>C