Canonical Allele Identifier: CA1693538977

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558733_21558736delinsTACG , CM000669.2:g.21558733_21558736delinsTACG	GRCh38
NC_000007.13:g.21598351_21598354delinsTACG , CM000669.1:g.21598351_21598354delinsTACG	GRCh37
NC_000007.12:g.21564876_21564879delinsTACG	NCBI36
NG_012886.2:g.20519_20522delinsTACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-69_496-66delinsTACG MANE Select	ENSP00000475939.1:n.496-69_496-66delinsTACG
ENST00000328843.10:c.496-69_496-66delinsTACG	ENSP00000330671.7:n.496-69_496-66delinsTACG
ENST00000409508.7:c.496-69_496-66delinsTACG	ENSP00000475939.1:n.496-69_496-66delinsTACG
ENST00000620169.4:c.496-69_496-66delinsTACG	ENSP00000481693.1:n.496-69_496-66delinsTACG
NM_001277115.1:c.496-69_496-66delinsTACG	NP_001264044.1:n.496-69_496-66delinsTACG
NM_001277115.2:c.496-69_496-66delinsTACG MANE Select	NP_001264044.1:n.496-69_496-66delinsTACG