Canonical Allele Identifier: CA2123413952

Gene: MYH6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23393536_23393548delinsATCCCCTTTAGGG , CM000676.2:g.23393536_23393548delinsATCCCCTTTAGGG	GRCh38
NC_000014.8:g.23862745_23862757delinsATCCCCTTTAGGG , CM000676.1:g.23862745_23862757delinsATCCCCTTTAGGG	GRCh37
NC_000014.7:g.22932585_22932597delinsATCCCCTTTAGGG	NCBI36
NG_023444.1:g.19730_19742delinsCCCTAAAGGGGAT , LRG_389:g.19730_19742delinsCCCTAAAGGGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405093.9:c.2929-30_2929-18delinsCCCTAAAGGGGAT MANE Select	ENSP00000386041.3:n.2929-30_2929-18delinsCCCTAAAGGGGAT
ENST00000356287.3:c.2929-30_2929-18delinsCCCTAAAGGGGAT	ENSP00000348634.3:n.2929-30_2929-18delinsCCCTAAAGGGGAT
ENST00000405093.7:c.2929-30_2929-18delinsCCCTAAAGGGGAT	ENSP00000386041.3:n.2929-30_2929-18delinsCCCTAAAGGGGAT
NM_002471.3:c.2929-30_2929-18delinsCCCTAAAGGGGAT , LRG_389t1:c.2929-30_2929-18delinsCCCTAAAGGGGAT	NP_002462.2:n.2929-30_2929-18delinsCCCTAAAGGGGAT
NM_002471.4:c.2929-30_2929-18delinsCCCTAAAGGGGAT MANE Select	NP_002462.2:n.2929-30_2929-18delinsCCCTAAAGGGGAT