Canonical Allele Identifier: CA453967958

Gene: DNAH11

Linked Data

• MyVariant Identifiers: chr7:g.21920487C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21880869C>T , CM000669.2:g.21880869C>T	GRCh38
NC_000007.13:g.21920487C>T , CM000669.1:g.21920487C>T	GRCh37
NC_000007.12:g.21887012C>T	NCBI36
NG_012886.2:g.342655C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12363C>T MANE Select	ENSP00000475939.1:p.Tyr4121=
ENST00000328843.10:c.12384C>T	ENSP00000330671.7:p.Tyr4128=
ENST00000409508.7:c.12363C>T	ENSP00000475939.1:p.Tyr4121=
ENST00000620169.4:c.12384C>T	ENSP00000481693.1:p.Tyr4128=
NM_001277115.1:c.12363C>T	NP_001264044.1:p.Tyr4121=
NM_001277115.2:c.12363C>T MANE Select	NP_001264044.1:p.Tyr4121=