Canonical Allele Identifier: CA2245965946

Gene: DNAH2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7730438T= , CM000679.2:g.7730438T=	GRCh38
NC_000017.10:g.7633756T= , CM000679.1:g.7633756T=	GRCh37
NC_000017.9:g.7574481T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000572933.6:c.400-2649T= MANE Select	ENSP00000458355.1:n.400-2649T=
ENST00000389173.6:c.400-2649T=	ENSP00000373825.2:n.400-2649T=
ENST00000570791.5:c.400-2649T=	ENSP00000460245.1:n.400-2649T=
ENST00000572933.5:c.400-2649T=	ENSP00000458355.1:n.400-2649T=
NM_001303270.1:c.400-2649T=	NP_001290199.1:n.400-2649T=
NM_020877.3:c.400-2649T=	NP_065928.2:n.400-2649T=
XM_011523663.1:c.400-2649T=	XP_011521965.1:n.400-2649T=
XM_011523664.1:c.400-2649T=	XP_011521966.1:n.400-2649T=
XM_011523665.1:c.400-2649T=	XP_011521967.1:n.400-2649T=
XM_011523666.1:c.400-2649T=	XP_011521968.1:n.400-2649T=
XM_011523667.1:c.400-2649T=	XP_011521969.1:n.400-2649T=
XM_011523670.1:c.400-2649T=	XP_011521972.1:n.400-2649T=
XM_011523667.2:c.400-2649T=	XP_011521969.1:n.400-2649T=
XM_011523670.2:c.400-2649T=	XP_011521972.1:n.400-2649T=
XM_017024219.1:c.400-2649T=	XP_016879708.1:n.400-2649T=
XM_024450604.1:c.400-2649T=	XP_024306372.1:n.400-2649T=
XM_024450605.1:c.400-2649T=	XP_024306373.1:n.400-2649T=
XM_024450606.1:c.400-2649T=	XP_024306374.1:n.400-2649T=
XM_024450607.1:c.400-2649T=	XP_024306375.1:n.400-2649T=
NM_001303270.2:c.400-2649T=	NP_001290199.1:n.400-2649T=
NM_020877.4:c.400-2649T=	NP_065928.2:n.400-2649T=
NM_020877.5:c.400-2649T= MANE Select	NP_065928.2:n.400-2649T=