Canonical Allele Identifier: CA2403795073

Gene: MYH9

Linked Data

• dbSNP Id: rs2016501495

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282215_36282220dup , CM000684.2:g.36282215_36282220dup	GRCh38
NC_000022.10:g.36678261_36678266dup , CM000684.1:g.36678261_36678266dup	GRCh37
NC_000022.9:g.35008207_35008212dup	NCBI36
NG_011884.2:g.110799_110804dup , LRG_567:g.110799_110804dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2764_2769dup
ENST00000685801.1:c.*448_*453dup	ENSP00000510688.1:n.*448_*453dup
ENST00000690244.1:n.1667_1672dup
ENST00000691109.1:n.6626_6631dup
ENST00000216181.11:c.*448_*453dup MANE Select	ENSP00000216181.6:n.*448_*453dup
ENST00000216181.9:c.*448_*453dup	ENSP00000216181.5:n.*448_*453dup
NM_002473.5:c.*448_*453dup , LRG_567t1:c.*448_*453dup	NP_002464.1:n.*448_*453dup
XM_011530197.1:c.*448_*453dup	XP_011528499.1:n.*448_*453dup
XM_011530197.2:c.*448_*453dup	XP_011528499.1:n.*448_*453dup
XM_017028803.1:c.*448_*453dup	XP_016884292.1:n.*448_*453dup
XM_017028804.1:c.*448_*453dup	XP_016884293.1:n.*448_*453dup
XM_017028805.1:c.*448_*453dup	XP_016884294.1:n.*448_*453dup
XM_017028806.1:c.*448_*453dup	XP_016884295.1:n.*448_*453dup
NM_002473.6:c.*448_*453dup MANE Select	NP_002464.1:n.*448_*453dup