Canonical Allele Identifier: CA1693712916

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21880924_21880927delinsAAGG , CM000669.2:g.21880924_21880927delinsAAGG	GRCh38
NC_000007.13:g.21920542_21920545delinsAAGG , CM000669.1:g.21920542_21920545delinsAAGG	GRCh37
NC_000007.12:g.21887067_21887070delinsAAGG	NCBI36
NG_012886.2:g.342710_342713delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12387+31_12387+34delinsAAGG MANE Select	ENSP00000475939.1:n.12387+31_12387+34delinsAAGG
ENST00000328843.10:c.12408+31_12408+34delinsAAGG	ENSP00000330671.7:n.12408+31_12408+34delinsAAGG
ENST00000409508.7:c.12387+31_12387+34delinsAAGG	ENSP00000475939.1:n.12387+31_12387+34delinsAAGG
ENST00000620169.4:c.12408+31_12408+34delinsAAGG	ENSP00000481693.1:n.12408+31_12408+34delinsAAGG
NM_001277115.1:c.12387+31_12387+34delinsAAGG	NP_001264044.1:n.12387+31_12387+34delinsAAGG
NM_001277115.2:c.12387+31_12387+34delinsAAGG MANE Select	NP_001264044.1:n.12387+31_12387+34delinsAAGG