Canonical Allele Identifier: CA155057929
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs771623831

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21543457G>C , CM000669.2:g.21543457G>C GRCh38
NC_000007.13:g.21583075G>C , CM000669.1:g.21583075G>C GRCh37
NC_000007.12:g.21549600G>C NCBI36
NG_012886.2:g.5243G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.212G>C MANE Select ENSP00000475939.1:p.Gly71Ala
ENST00000328843.10:c.212G>C ENSP00000330671.7:p.Gly71Ala
ENST00000409508.7:c.212G>C ENSP00000475939.1:p.Gly71Ala
ENST00000607050.1:n.12G>C
ENST00000620169.4:c.212G>C ENSP00000481693.1:p.Gly71Ala
NM_001277115.1:c.212G>C NP_001264044.1:p.Gly71Ala
NM_001277115.2:c.212G>C MANE Select NP_001264044.1:p.Gly71Ala