Canonical Allele Identifier: CA1693712880
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880888T= , CM000669.2:g.21880888T= GRCh38
NC_000007.13:g.21920506T= , CM000669.1:g.21920506T= GRCh37
NC_000007.12:g.21887031T= NCBI36
NG_012886.2:g.342674T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12382T= MANE Select ENSP00000475939.1:p.Ser4128=
ENST00000328843.10:c.12403T= ENSP00000330671.7:p.Ser4135=
ENST00000409508.7:c.12382T= ENSP00000475939.1:p.Ser4128=
ENST00000620169.4:c.12403T= ENSP00000481693.1:p.Ser4135=
NM_001277115.1:c.12382T= NP_001264044.1:p.Ser4128=
NM_001277115.2:c.12382T= MANE Select NP_001264044.1:p.Ser4128=