Canonical Allele Identifier: CA2499935441

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36316730_36316731insCATATTGTTAGATATTAGGTTGTTTGTACTTTTCA , CM000684.2:g.36316730_36316731insCATATTGTTAGATATTAGGTTGTTTGTACTTTTCA	GRCh38
NC_000022.10:g.36712775_36712776insCATATTGTTAGATATTAGGTTGTTTGTACTTTTCA , CM000684.1:g.36712775_36712776insCATATTGTTAGATATTAGGTTGTTTGTACTTTTCA	GRCh37
NC_000022.9:g.35042721_35042722insCATATTGTTAGATATTAGGTTGTTTGTACTTTTCA	NCBI36
NG_011884.2:g.76288_76289insTGAAAAGTACAAACAACCTAATATCTAACAATATG , LRG_567:g.76288_76289insTGAAAAGTACAAACAACCTAATATCTAACAATATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685187.1:n.1442-62_1442-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG
ENST00000685801.1:c.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG	ENSP00000510688.1:n.1228-62_1228-61insTGAAAAGTACAAACAACCTAATA...
ENST00000691109.1:n.1523-62_1523-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG
ENST00000691687.1:n.2026-62_2026-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG
ENST00000692930.1:n.1442-62_1442-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG
ENST00000216181.11:c.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG MANE Select	ENSP00000216181.6:n.1228-62_1228-61insTGAAAAGTACAAACAACCTAATA...
ENST00000216181.9:c.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG	ENSP00000216181.5:n.1228-62_1228-61insTGAAAAGTACAAACAACCTAATA...
ENST00000477189.1:n.416-62_416-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG
NM_002473.5:c.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG , LRG_567t1:c.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG	NP_002464.1:n.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAAC...
XM_011530197.1:c.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG	XP_011528499.1:n.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCT...
XM_011530197.2:c.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG	XP_011528499.1:n.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCT...
XM_017028803.1:c.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG	XP_016884292.1:n.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCT...
XM_017028804.1:c.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG	XP_016884293.1:n.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCT...
XM_017028805.1:c.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG	XP_016884294.1:n.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCT...
XM_017028806.1:c.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG	XP_016884295.1:n.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCT...
NM_002473.6:c.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAACAATATG MANE Select	NP_002464.1:n.1228-62_1228-61insTGAAAAGTACAAACAACCTAATATCTAAC...