Canonical Allele Identifier: CA453965823
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21893995G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21854377G>A , CM000669.2:g.21854377G>A GRCh38
NC_000007.13:g.21893995G>A , CM000669.1:g.21893995G>A GRCh37
NC_000007.12:g.21860520G>A NCBI36
NG_012886.2:g.316163G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.11124G>A MANE Select ENSP00000475939.1:p.Val3708=
ENST00000328843.10:c.11145G>A ENSP00000330671.7:p.Val3715=
ENST00000409508.7:c.11124G>A ENSP00000475939.1:p.Val3708=
ENST00000421290.1:n.307G>A
ENST00000607413.5:n.387G>A
ENST00000620169.4:c.11145G>A ENSP00000481693.1:p.Val3715=
NM_001277115.1:c.11124G>A NP_001264044.1:p.Val3708=
NM_001277115.2:c.11124G>A MANE Select NP_001264044.1:p.Val3708=
Search 100 bp 5'
Search 100 bp 3'