Canonical Allele Identifier: CA366948479
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21856183A>T (hg19) chr7:g.21816565A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816565A>T , CM000669.2:g.21816565A>T GRCh38
NC_000007.13:g.21856183A>T , CM000669.1:g.21856183A>T GRCh37
NC_000007.12:g.21822708A>T NCBI36
NG_012886.2:g.278351A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10431A>T MANE Select ENSP00000475939.1:p.Arg3477Ser
ENST00000328843.10:c.10452A>T ENSP00000330671.7:p.Arg3484Ser
ENST00000409508.7:c.10431A>T ENSP00000475939.1:p.Arg3477Ser
ENST00000620169.4:c.10452A>T ENSP00000481693.1:p.Arg3484Ser
NM_001277115.1:c.10431A>T NP_001264044.1:p.Arg3477Ser
NM_001277115.2:c.10431A>T MANE Select NP_001264044.1:p.Arg3477Ser
Search 100 bp 5'
Search 100 bp 3'