Canonical Allele Identifier: CA366964001

Gene: DNAH11

Linked Data

• COSMIC: COSM6433125 ; COSM6433126
• MyVariant Identifiers: chr7:g.21920390C>T (hg19) ; chr7:g.21880772C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21880772C>T , CM000669.2:g.21880772C>T	GRCh38
NC_000007.13:g.21920390C>T , CM000669.1:g.21920390C>T	GRCh37
NC_000007.12:g.21886915C>T	NCBI36
NG_012886.2:g.342558C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.12266C>T MANE Select	ENSP00000475939.1:p.Ala4089Val
ENST00000328843.10:c.12287C>T	ENSP00000330671.7:p.Ala4096Val
ENST00000409508.7:c.12266C>T	ENSP00000475939.1:p.Ala4089Val
ENST00000620169.4:c.12287C>T	ENSP00000481693.1:p.Ala4096Val
NM_001277115.1:c.12266C>T	NP_001264044.1:p.Ala4089Val
NM_001277115.2:c.12266C>T MANE Select	NP_001264044.1:p.Ala4089Val