Canonical Allele Identifier: CA453968503
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21748652-G-A
MyVariant Identifiers: chr7:g.21788270G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748652G>A , CM000669.2:g.21748652G>A GRCh38
NC_000007.13:g.21788270G>A , CM000669.1:g.21788270G>A GRCh37
NC_000007.12:g.21754795G>A NCBI36
NG_012886.2:g.210438G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8583G>A MANE Select ENSP00000475939.1:p.Lys2861=
ENST00000328843.10:c.8604G>A ENSP00000330671.7:p.Lys2868=
ENST00000409508.7:c.8583G>A ENSP00000475939.1:p.Lys2861=
ENST00000620169.4:c.8604G>A ENSP00000481693.1:p.Lys2868=
NM_001277115.1:c.8583G>A NP_001264044.1:p.Lys2861=
NM_001277115.2:c.8583G>A MANE Select NP_001264044.1:p.Lys2861=
Search 100 bp 5'
Search 100 bp 3'