Canonical Allele Identifier: CA4183048
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs200590825
gnomAD v2: 7-21920505-C-T
gnomAD v4: 7-21880887-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880887C>T , CM000669.2:g.21880887C>T GRCh38
NC_000007.13:g.21920505C>T , CM000669.1:g.21920505C>T GRCh37
NC_000007.12:g.21887030C>T NCBI36
NG_012886.2:g.342673C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12381C>T MANE Select ENSP00000475939.1:p.Asn4127=
ENST00000328843.10:c.12402C>T ENSP00000330671.7:p.Asn4134=
ENST00000409508.7:c.12381C>T ENSP00000475939.1:p.Asn4127=
ENST00000620169.4:c.12402C>T ENSP00000481693.1:p.Asn4134=
NM_001277115.1:c.12381C>T NP_001264044.1:p.Asn4127=
NM_001277115.2:c.12381C>T MANE Select NP_001264044.1:p.Asn4127=