Canonical Allele Identifier: CA1693538914

Gene: DNAH11

Linked Data

• dbSNP Id: rs1783318586

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558695_21558696insGTG , CM000669.2:g.21558695_21558696insGTG	GRCh38
NC_000007.13:g.21598313_21598314insGTG , CM000669.1:g.21598313_21598314insGTG	GRCh37
NC_000007.12:g.21564838_21564839insGTG	NCBI36
NG_012886.2:g.20481_20482insGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-107_496-106insGTG MANE Select	ENSP00000475939.1:n.496-107_496-106insGTG
ENST00000328843.10:c.496-107_496-106insGTG	ENSP00000330671.7:n.496-107_496-106insGTG
ENST00000409508.7:c.496-107_496-106insGTG	ENSP00000475939.1:n.496-107_496-106insGTG
ENST00000620169.4:c.496-107_496-106insGTG	ENSP00000481693.1:n.496-107_496-106insGTG
NM_001277115.1:c.496-107_496-106insGTG	NP_001264044.1:n.496-107_496-106insGTG
NM_001277115.2:c.496-107_496-106insGTG MANE Select	NP_001264044.1:n.496-107_496-106insGTG