Canonical Allele Identifier: CA366959744

Gene: DNAH11

Linked Data

• MyVariant Identifiers: chr7:g.21893945A>T (hg19) ; chr7:g.21854327A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21854327A>T , CM000669.2:g.21854327A>T	GRCh38
NC_000007.13:g.21893945A>T , CM000669.1:g.21893945A>T	GRCh37
NC_000007.12:g.21860470A>T	NCBI36
NG_012886.2:g.316113A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.11074A>T MANE Select	ENSP00000475939.1:p.Lys3692Ter
ENST00000328843.10:c.11095A>T	ENSP00000330671.7:p.Lys3699Ter
ENST00000409508.7:c.11074A>T	ENSP00000475939.1:p.Lys3692Ter
ENST00000421290.1:n.257A>T
ENST00000607413.5:n.337A>T
ENST00000620169.4:c.11095A>T	ENSP00000481693.1:p.Lys3699Ter
NM_001277115.1:c.11074A>T	NP_001264044.1:p.Lys3692Ter
NM_001277115.2:c.11074A>T MANE Select	NP_001264044.1:p.Lys3692Ter