Canonical Allele Identifier: CA155074160

Gene: DNAH11

Linked Data

• dbSNP Id: rs34817693
• MyVariant Identifiers: chr7:g.21598313_21598314insGAT (hg19) ; chr7:g.21558695_21558696insGAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558695_21558696insGAT , CM000669.2:g.21558695_21558696insGAT	GRCh38
NC_000007.13:g.21598313_21598314insGAT , CM000669.1:g.21598313_21598314insGAT	GRCh37
NC_000007.12:g.21564838_21564839insGAT	NCBI36
NG_012886.2:g.20481_20482insGAT

Transcript Alleles

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