Canonical Allele Identifier: CA2681986989

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21748487-TCAAAAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21748492_21748497del , CM000669.2:g.21748492_21748497del	GRCh38
NC_000007.13:g.21788110_21788115del , CM000669.1:g.21788110_21788115del	GRCh37
NC_000007.12:g.21754635_21754640del	NCBI36
NG_012886.2:g.210278_210283del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.8511-88_8511-83del MANE Select	ENSP00000475939.1:n.8511-88_8511-83del
ENST00000328843.10:c.8532-88_8532-83del	ENSP00000330671.7:n.8532-88_8532-83del
ENST00000409508.7:c.8511-88_8511-83del	ENSP00000475939.1:n.8511-88_8511-83del
ENST00000620169.4:c.8532-88_8532-83del	ENSP00000481693.1:n.8532-88_8532-83del
NM_001277115.1:c.8511-88_8511-83del	NP_001264044.1:n.8511-88_8511-83del
NM_001277115.2:c.8511-88_8511-83del MANE Select	NP_001264044.1:n.8511-88_8511-83del