Canonical Allele Identifier: CA2578843331

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21748494-CAAAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21748506_21748509del , CM000669.2:g.21748506_21748509del	GRCh38
NC_000007.13:g.21788124_21788127del , CM000669.1:g.21788124_21788127del	GRCh37
NC_000007.12:g.21754649_21754652del	NCBI36
NG_012886.2:g.210292_210295del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.8511-74_8511-71del MANE Select	ENSP00000475939.1:n.8511-74_8511-71del
ENST00000328843.10:c.8532-74_8532-71del	ENSP00000330671.7:n.8532-74_8532-71del
ENST00000409508.7:c.8511-74_8511-71del	ENSP00000475939.1:n.8511-74_8511-71del
ENST00000620169.4:c.8532-74_8532-71del	ENSP00000481693.1:n.8532-74_8532-71del
NM_001277115.1:c.8511-74_8511-71del	NP_001264044.1:n.8511-74_8511-71del
NM_001277115.2:c.8511-74_8511-71del MANE Select	NP_001264044.1:n.8511-74_8511-71del