Canonical Allele Identifier: CA454138934
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21583076G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21543458G>C , CM000669.2:g.21543458G>C GRCh38
NC_000007.13:g.21583076G>C , CM000669.1:g.21583076G>C GRCh37
NC_000007.12:g.21549601G>C NCBI36
NG_012886.2:g.5244G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.213G>C MANE Select ENSP00000475939.1:p.Gly71=
ENST00000328843.10:c.213G>C ENSP00000330671.7:p.Gly71=
ENST00000409508.7:c.213G>C ENSP00000475939.1:p.Gly71=
ENST00000607050.1:n.13G>C
ENST00000620169.4:c.213G>C ENSP00000481693.1:p.Gly71=
NM_001277115.1:c.213G>C NP_001264044.1:p.Gly71=
NM_001277115.2:c.213G>C MANE Select NP_001264044.1:p.Gly71=
Search 100 bp 5'
Search 100 bp 3'