Canonical Allele Identifier: CA2681989684

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21816791-TCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21816796_21816798del , CM000669.2:g.21816796_21816798del	GRCh38
NC_000007.13:g.21856414_21856416del , CM000669.1:g.21856414_21856416del	GRCh37
NC_000007.12:g.21822939_21822941del	NCBI36
NG_012886.2:g.278582_278584del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10568+94_10568+96del MANE Select	ENSP00000475939.1:n.10568+94_10568+96del
ENST00000328843.10:c.10589+94_10589+96del	ENSP00000330671.7:n.10589+94_10589+96del
ENST00000409508.7:c.10568+94_10568+96del	ENSP00000475939.1:n.10568+94_10568+96del
ENST00000620169.4:c.10589+94_10589+96del	ENSP00000481693.1:n.10589+94_10589+96del
NM_001277115.1:c.10568+94_10568+96del	NP_001264044.1:n.10568+94_10568+96del
NM_001277115.2:c.10568+94_10568+96del MANE Select	NP_001264044.1:n.10568+94_10568+96del