Canonical Allele Identifier: CA1693539320
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21558891G= , CM000669.2:g.21558891G= GRCh38
NC_000007.13:g.21598509G= , CM000669.1:g.21598509G= GRCh37
NC_000007.12:g.21565034G= NCBI36
NG_012886.2:g.20677G=

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.585G= MANE Select ENSP00000475939.1:p.Met195=
ENST00000328843.10:c.585G= ENSP00000330671.7:p.Met195=
ENST00000409508.7:c.585G= ENSP00000475939.1:p.Met195=
ENST00000620169.4:c.585G= ENSP00000481693.1:p.Met195=
NM_001277115.1:c.585G= NP_001264044.1:p.Met195=
NM_001277115.2:c.585G= MANE Select NP_001264044.1:p.Met195=