Canonical Allele Identifier: CA572927359

Gene: DNAH11

Linked Data

• dbSNP Id: rs1267625205
• gnomAD v2: 7-21920874-CATAACACTGCATTA-C
• gnomAD v3: 7-21881256-CATAACACTGCATTA-C
• gnomAD v4: 7-21881256-CATAACACTGCATTA-C
• MyVariant Identifiers: chr7:g.21920875_21920888del (hg19) ; chr7:g.21881257_21881270del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21881261_21881274del , CM000669.2:g.21881261_21881274del	GRCh38
NC_000007.13:g.21920879_21920892del , CM000669.1:g.21920879_21920892del	GRCh37
NC_000007.12:g.21887404_21887417del	NCBI36
NG_012886.2:g.343047_343060del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12387+368_12387+381del MANE Select	ENSP00000475939.1:n.12387+368_12387+381del
ENST00000328843.10:c.12408+368_12408+381del	ENSP00000330671.7:n.12408+368_12408+381del
ENST00000409508.7:c.12387+368_12387+381del	ENSP00000475939.1:n.12387+368_12387+381del
ENST00000620169.4:c.12408+368_12408+381del	ENSP00000481693.1:n.12408+368_12408+381del
NM_001277115.1:c.12387+368_12387+381del	NP_001264044.1:n.12387+368_12387+381del
NM_001277115.2:c.12387+368_12387+381del MANE Select	NP_001264044.1:n.12387+368_12387+381del