Canonical Allele Identifier: CA2713854728
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1226717098
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21567573C>T , CM000669.2:g.21567573C>T GRCh38
NC_000007.13:g.21607191C>T , CM000669.1:g.21607191C>T GRCh37
NC_000007.12:g.21573716C>T NCBI36
NG_012886.2:g.29359C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.1195-2496C>T MANE Select ENSP00000475939.1:n.1195-2496C>T
ENST00000328843.10:c.1195-2496C>T ENSP00000330671.7:n.1195-2496C>T
ENST00000409508.7:c.1195-2496C>T ENSP00000475939.1:n.1195-2496C>T
ENST00000496218.1:n.81-2496C>T
ENST00000620169.4:c.1195-2496C>T ENSP00000481693.1:n.1195-2496C>T
NM_001277115.1:c.1195-2496C>T NP_001264044.1:n.1195-2496C>T
XR_927090.1:n.563+5753G>A
XR_001745114.1:n.2793+5753G>A
NM_001277115.2:c.1195-2496C>T MANE Select NP_001264044.1:n.1195-2496C>T
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