Canonical Allele Identifier: CA366955484
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21748720-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748720G>C , CM000669.2:g.21748720G>C GRCh38
NC_000007.13:g.21788338G>C , CM000669.1:g.21788338G>C GRCh37
NC_000007.12:g.21754863G>C NCBI36
NG_012886.2:g.210506G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8651G>C MANE Select ENSP00000475939.1:p.Gly2884Ala
ENST00000328843.10:c.8672G>C ENSP00000330671.7:p.Gly2891Ala
ENST00000409508.7:c.8651G>C ENSP00000475939.1:p.Gly2884Ala
ENST00000620169.4:c.8672G>C ENSP00000481693.1:p.Gly2891Ala
NM_001277115.1:c.8651G>C NP_001264044.1:p.Gly2884Ala
NM_001277115.2:c.8651G>C MANE Select NP_001264044.1:p.Gly2884Ala