Canonical Allele Identifier: CA1693713212
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1783914559

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21881253G>C , CM000669.2:g.21881253G>C GRCh38
NC_000007.13:g.21920871G>C , CM000669.1:g.21920871G>C GRCh37
NC_000007.12:g.21887396G>C NCBI36
NG_012886.2:g.343039G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12387+360G>C MANE Select ENSP00000475939.1:n.12387+360G>C
ENST00000328843.10:c.12408+360G>C ENSP00000330671.7:n.12408+360G>C
ENST00000409508.7:c.12387+360G>C ENSP00000475939.1:n.12387+360G>C
ENST00000620169.4:c.12408+360G>C ENSP00000481693.1:n.12408+360G>C
NM_001277115.1:c.12387+360G>C NP_001264044.1:n.12387+360G>C
NM_001277115.2:c.12387+360G>C MANE Select NP_001264044.1:n.12387+360G>C