Canonical Allele Identifier: CA366932394
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21598488G>T (hg19) chr7:g.21558870G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21558870G>T , CM000669.2:g.21558870G>T GRCh38
NC_000007.13:g.21598488G>T , CM000669.1:g.21598488G>T GRCh37
NC_000007.12:g.21565013G>T NCBI36
NG_012886.2:g.20656G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.564G>T MANE Select ENSP00000475939.1:p.Met188Ile
ENST00000328843.10:c.564G>T ENSP00000330671.7:p.Met188Ile
ENST00000409508.7:c.564G>T ENSP00000475939.1:p.Met188Ile
ENST00000620169.4:c.564G>T ENSP00000481693.1:p.Met188Ile
NM_001277115.1:c.564G>T NP_001264044.1:p.Met188Ile
NM_001277115.2:c.564G>T MANE Select NP_001264044.1:p.Met188Ile
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