Canonical Allele Identifier: CA366959974
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21854378-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21854378G>T , CM000669.2:g.21854378G>T GRCh38
NC_000007.13:g.21893996G>T , CM000669.1:g.21893996G>T GRCh37
NC_000007.12:g.21860521G>T NCBI36
NG_012886.2:g.316164G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.11125G>T MANE Select ENSP00000475939.1:p.Ala3709Ser
ENST00000328843.10:c.11146G>T ENSP00000330671.7:p.Ala3716Ser
ENST00000409508.7:c.11125G>T ENSP00000475939.1:p.Ala3709Ser
ENST00000421290.1:n.308G>T
ENST00000607413.5:n.388G>T
ENST00000620169.4:c.11146G>T ENSP00000481693.1:p.Ala3716Ser
NM_001277115.1:c.11125G>T NP_001264044.1:p.Ala3709Ser
NM_001277115.2:c.11125G>T MANE Select NP_001264044.1:p.Ala3709Ser