Canonical Allele Identifier: CA366955176
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21788265G>T (hg19) chr7:g.21748647G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748647G>T , CM000669.2:g.21748647G>T GRCh38
NC_000007.13:g.21788265G>T , CM000669.1:g.21788265G>T GRCh37
NC_000007.12:g.21754790G>T NCBI36
NG_012886.2:g.210433G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8578G>T MANE Select ENSP00000475939.1:p.Gly2860Cys
ENST00000328843.10:c.8599G>T ENSP00000330671.7:p.Gly2867Cys
ENST00000409508.7:c.8578G>T ENSP00000475939.1:p.Gly2860Cys
ENST00000620169.4:c.8599G>T ENSP00000481693.1:p.Gly2867Cys
NM_001277115.1:c.8578G>T NP_001264044.1:p.Gly2860Cys
NM_001277115.2:c.8578G>T MANE Select NP_001264044.1:p.Gly2860Cys
Search 100 bp 5'
Search 100 bp 3'