Canonical Allele Identifier: CA2487035801

Gene: ACTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236719138_236719151delinsTCTCTCTTAGGGCG , CM000663.2:g.236719138_236719151delinsTCTCTCTTAGGGCG	GRCh38
NC_000001.10:g.236882438_236882451delinsTCTCTCTTAGGGCG , CM000663.1:g.236882438_236882451delinsTCTCTCTTAGGGCG	GRCh37
NC_000001.9:g.234949061_234949074delinsTCTCTCTTAGGGCG	NCBI36
NG_009081.1:g.37669_37682delinsTCTCTCTTAGGGCG
NG_009081.2:g.59998_60011delinsTCTCTCTTAGGGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.361+125_361+138delinsTCTCTCTTAGGGCG	ENSP00000443495.1:n.361+125_361+138delinsTCTCTCTTAGGGCG
ENST00000492634.7:n.456+125_456+138delinsTCTCTCTTAGGGCG
ENST00000494762.2:n.110+125_110+138delinsTCTCTCTTAGGGCG
ENST00000682015.1:c.361+125_361+138delinsTCTCTCTTAGGGCG	ENSP00000506961.1:n.361+125_361+138delinsTCTCTCTTAGGGCG
ENST00000682692.1:n.361+125_361+138delinsTCTCTCTTAGGGCG
ENST00000682966.1:n.360+125_360+138delinsTCTCTCTTAGGGCG
ENST00000683075.1:n.300+125_300+138delinsTCTCTCTTAGGGCG
ENST00000683111.1:c.304+125_304+138delinsTCTCTCTTAGGGCG	ENSP00000507913.1:n.304+125_304+138delinsTCTCTCTTAGGGCG
ENST00000684050.1:n.396+125_396+138delinsTCTCTCTTAGGGCG
ENST00000684286.1:n.429+125_429+138delinsTCTCTCTTAGGGCG
ENST00000684502.1:n.396+125_396+138delinsTCTCTCTTAGGGCG
ENST00000366578.6:c.361+125_361+138delinsTCTCTCTTAGGGCG MANE Select	ENSP00000355537.4:n.361+125_361+138delinsTCTCTCTTAGGGCG
ENST00000492634.6:n.456+125_456+138delinsTCTCTCTTAGGGCG
ENST00000542672.6:c.361+125_361+138delinsTCTCTCTTAGGGCG	ENSP00000443495.1:n.361+125_361+138delinsTCTCTCTTAGGGCG
ENST00000651091.1:c.304+125_304+138delinsTCTCTCTTAGGGCG	ENSP00000498677.1:n.304+125_304+138delinsTCTCTCTTAGGGCG
ENST00000651187.1:c.145+125_145+138delinsTCTCTCTTAGGGCG	ENSP00000498348.1:n.145+125_145+138delinsTCTCTCTTAGGGCG
ENST00000651275.1:c.346+125_346+138delinsTCTCTCTTAGGGCG	ENSP00000498926.1:n.346+125_346+138delinsTCTCTCTTAGGGCG
ENST00000651786.1:c.361+125_361+138delinsTCTCTCTTAGGGCG	ENSP00000498364.1:n.361+125_361+138delinsTCTCTCTTAGGGCG
ENST00000652096.1:c.361+125_361+138delinsTCTCTCTTAGGGCG	ENSP00000498896.1:n.361+125_361+138delinsTCTCTCTTAGGGCG
ENST00000366578.5:c.361+125_361+138delinsTCTCTCTTAGGGCG	ENSP00000355537.4:n.361+125_361+138delinsTCTCTCTTAGGGCG
ENST00000492634.5:n.508+125_508+138delinsTCTCTCTTAGGGCG
ENST00000542672.5:c.361+125_361+138delinsTCTCTCTTAGGGCG	ENSP00000443495.1:n.361+125_361+138delinsTCTCTCTTAGGGCG
ENST00000546208.5:c.-461+125_-461+138delinsTCTCTCTTAGGGCG	ENSP00000438384.2:n.-461+125_-461+138delinsTCTCTCTTAGGGCG
NM_001103.3:c.361+125_361+138delinsTCTCTCTTAGGGCG	NP_001094.1:n.361+125_361+138delinsTCTCTCTTAGGGCG
NM_001278343.1:c.361+125_361+138delinsTCTCTCTTAGGGCG	NP_001265272.1:n.361+125_361+138delinsTCTCTCTTAGGGCG
NM_001278344.1:c.-461+125_-461+138delinsTCTCTCTTAGGGCG	NP_001265273.1:n.-461+125_-461+138delinsTCTCTCTTAGGGCG
NM_001278343.2:c.361+125_361+138delinsTCTCTCTTAGGGCG	NP_001265272.1:n.361+125_361+138delinsTCTCTCTTAGGGCG
NM_001103.4:c.361+125_361+138delinsTCTCTCTTAGGGCG MANE Select	NP_001094.1:n.361+125_361+138delinsTCTCTCTTAGGGCG
NM_001278344.2:c.-461+125_-461+138delinsTCTCTCTTAGGGCG	NP_001265273.1:n.-461+125_-461+138delinsTCTCTCTTAGGGCG