Canonical Allele Identifier: CA2695230755

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36296899_36296919del , CM000684.2:g.36296899_36296919del	GRCh38
NC_000022.10:g.36692945_36692965del , CM000684.1:g.36692945_36692965del	GRCh37
NC_000022.9:g.35022891_35022911del	NCBI36
NG_011884.2:g.96106_96126del , LRG_567:g.96106_96126del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685801.1:c.3265_3285del	ENSP00000510688.1:p.Gln1089_Leu1095del
ENST00000691109.1:n.3497_3517del
ENST00000216181.11:c.3202_3222del MANE Select	ENSP00000216181.6:p.Gln1068_Leu1074del
ENST00000216181.9:c.3202_3222del	ENSP00000216181.5:p.Gln1068_Leu1074del
ENST00000459960.1:n.411_431del
NM_002473.5:c.3202_3222del , LRG_567t1:c.3202_3222del	NP_002464.1:p.Gln1068_Leu1074del
XM_011530197.1:c.3202_3222del	XP_011528499.1:p.Gln1068_Leu1074del
XM_011530197.2:c.3202_3222del	XP_011528499.1:p.Gln1068_Leu1074del
XM_017028803.1:c.3202_3222del	XP_016884292.1:p.Gln1068_Leu1074del
XM_017028804.1:c.3202_3222del	XP_016884293.1:p.Gln1068_Leu1074del
XM_017028805.1:c.3202_3222del	XP_016884294.1:p.Gln1068_Leu1074del
XM_017028806.1:c.3202_3222del	XP_016884295.1:p.Gln1068_Leu1074del
NM_002473.6:c.3202_3222del MANE Select	NP_002464.1:p.Gln1068_Leu1074del