Canonical Allele Identifier: CA366948229
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21856139G>T (hg19) chr7:g.21816521G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816521G>T , CM000669.2:g.21816521G>T GRCh38
NC_000007.13:g.21856139G>T , CM000669.1:g.21856139G>T GRCh37
NC_000007.12:g.21822664G>T NCBI36
NG_012886.2:g.278307G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10387G>T MANE Select ENSP00000475939.1:p.Ala3463Ser
ENST00000328843.10:c.10408G>T ENSP00000330671.7:p.Ala3470Ser
ENST00000409508.7:c.10387G>T ENSP00000475939.1:p.Ala3463Ser
ENST00000620169.4:c.10408G>T ENSP00000481693.1:p.Ala3470Ser
NM_001277115.1:c.10387G>T NP_001264044.1:p.Ala3463Ser
NM_001277115.2:c.10387G>T MANE Select NP_001264044.1:p.Ala3463Ser
Search 100 bp 5'
Search 100 bp 3'