Canonical Allele Identifier: CA2144501716

Gene: ACTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68874131G= , CM000676.2:g.68874131G=	GRCh38
NC_000014.8:g.69340848G= , CM000676.1:g.69340848G=	GRCh37
NC_000014.7:g.68410601G=	NCBI36
NG_029480.1:g.110236C= , LRG_886:g.110236C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394419.9:c.*728C= MANE Select	ENSP00000377941.4:n.*728C=
NM_001102.3:c.*728C=	NP_001093.1:n.*728C=
NM_001130004.1:c.*728C= , LRG_886t1:c.*728C=	NP_001123476.1:n.*728C=
NM_001130005.1:c.*728C=	NP_001123477.1:n.*728C=
XM_011537265.1:c.*728C=	XP_011535567.1:n.*728C=
XM_011537266.1:c.*728C=	XP_011535568.1:n.*728C=
XM_011537267.1:c.*728C=	XP_011535569.1:n.*728C=
XM_011537268.1:c.*728C=	XP_011535570.1:n.*728C=
XM_011537269.1:c.*728C=	XP_011535571.1:n.*728C=
XM_011537270.1:c.*728C=	XP_011535572.1:n.*728C=
XM_011537271.1:c.*728C=	XP_011535573.1:n.*728C=
XM_011537265.2:c.*728C=	XP_011535567.1:n.*728C=
XM_011537266.3:c.*728C=	XP_011535568.1:n.*728C=
XM_011537267.3:c.*728C=	XP_011535569.1:n.*728C=
XM_011537268.3:c.*728C=	XP_011535570.1:n.*728C=
XM_017021720.1:c.*728C=	XP_016877209.1:n.*728C=
XM_017021722.2:c.*728C=	XP_016877211.1:n.*728C=
XM_017021725.1:c.*728C=	XP_016877214.1:n.*728C=
XM_017021727.2:c.*728C=	XP_016877216.1:n.*728C=
XM_017021728.2:c.*728C=	XP_016877217.1:n.*728C=
NM_001102.4:c.*728C=	NP_001093.1:n.*728C=
NM_001130005.2:c.*728C=	NP_001123477.1:n.*728C=
NM_001130004.2:c.*728C= MANE Select	NP_001123476.1:n.*728C=