Canonical Allele Identifier: CA366931133
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs2285943
MyVariant Identifiers: chr7:g.21582963G>A (hg19) chr7:g.21543345G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21543345G>A , CM000669.2:g.21543345G>A GRCh38
NC_000007.13:g.21582963G>A , CM000669.1:g.21582963G>A GRCh37
NC_000007.12:g.21549488G>A NCBI36
NG_012886.2:g.5131G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.100G>A MANE Select ENSP00000475939.1:p.Glu34Lys
ENST00000328843.10:c.100G>A ENSP00000330671.7:p.Glu34Lys
ENST00000409508.7:c.100G>A ENSP00000475939.1:p.Glu34Lys
ENST00000620169.4:c.100G>A ENSP00000481693.1:p.Glu34Lys
NM_001277115.1:c.100G>A NP_001264044.1:p.Glu34Lys
NM_001277115.2:c.100G>A MANE Select NP_001264044.1:p.Glu34Lys
Search 100 bp 5'
Search 100 bp 3'