Canonical Allele Identifier: CA4182229

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21801201G>T , CM000669.2:g.21801201G>T	GRCh38
NC_000007.13:g.21840819G>T , CM000669.1:g.21840819G>T	GRCh37
NC_000007.12:g.21807344G>T	NCBI36
NG_012886.2:g.262987G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001277115.2:c.10091G>T MANE Select	NP_001264044.1:p.Arg3364Leu
ENST00000409508.8:c.10091G>T MANE Select	ENSP00000475939.1:p.Arg3364Leu
NM_001277115.1:c.10091G>T	NP_001264044.1:p.Arg3364Leu
ENST00000328843.10:c.10112G>T	ENSP00000330671.7:p.Arg3371Leu
ENST00000409508.7:c.10091G>T	ENSP00000475939.1:p.Arg3364Leu
ENST00000620169.4:c.10112G>T	ENSP00000481693.1:p.Arg3371Leu