Canonical Allele Identifier: CA1392018534

Gene: MYH15

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.108428881T= , CM000665.2:g.108428881T=	GRCh38
NC_000003.11:g.108147728T= , CM000665.1:g.108147728T=	GRCh37
NC_000003.10:g.109630418T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014981.3:c.3313A= MANE Select	NP_055796.2:p.Thr1105=
ENST00000693548.1:c.3313A= MANE Select	ENSP00000508967.1:p.Thr1105=
NM_014981.1:c.3373A=	NP_055796.1:p.Thr1125=
NM_014981.2:c.3373A=	NP_055796.1:p.Thr1125=
ENST00000273353.3:c.3373A=	ENSP00000273353.3:p.Thr1125=
ENST00000273353.4:c.3373A=	ENSP00000273353.3:p.Thr1125=
ENST00000273353.5:c.3313A=	ENSP00000273353.4:p.Thr1105=
ENST00000478998.5:n.1365A=
ENST00000689784.1:c.2332A=	ENSP00000509841.1:p.Thr778=
XM_011512559.1:c.3373A=	XP_011510861.1:p.Thr1125=
XM_011512559.2:c.3373A=	XP_011510861.1:p.Thr1125=
XM_017005922.1:c.2332A=	XP_016861411.1:p.Thr778=