Canonical Allele Identifier: CA2806179912

Gene: ACSM1 ACSM3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20663243dup , CM000678.2:g.20663243dup	GRCh38
NC_000016.9:g.20674565dup , CM000678.1:g.20674565dup	GRCh37
NC_000016.8:g.20582066dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000520010.6:c.913-1370dup (ACSM1) MANE Select	ENSP00000428047.1:n.913-1370dup
ENST00000307493.8:c.913-1370dup (ACSM1)	ENSP00000301956.3:n.913-1370dup
ENST00000519031.5:n.339-1370dup (ACSM1)
ENST00000519745.5:c.*359-1370dup (ACSM1)	ENSP00000428650.1:n.*359-1370dup
ENST00000520010.5:c.913-1370dup (ACSM1)	ENSP00000428047.1:n.913-1370dup
ENST00000524149.5:c.30-1370dup (ACSM1)
ENST00000568235.5:c.-190+52933dup (ACSM3)	ENSP00000457003.1:n.-190+52933dup
NM_052956.2:c.913-1370dup (ACSM1)	NP_443188.2:n.913-1370dup
XM_005255084.1:c.913-1370dup (ACSM1)	XP_005255141.1:n.913-1370dup
XM_006721016.1:c.913-1370dup (ACSM1)	XP_006721079.1:n.913-1370dup
XM_006721017.1:c.913-1370dup (ACSM1)	XP_006721080.1:n.913-1370dup
XM_006721018.1:c.253-1370dup (ACSM1)	XP_006721081.1:n.253-1370dup
XM_011545729.1:c.913-1370dup (ACSM1)	XP_011544031.1:n.913-1370dup
XM_011545730.1:c.913-1370dup (ACSM1)	XP_011544032.1:n.913-1370dup
XM_011545731.1:c.316-1370dup (ACSM1)	XP_011544033.1:n.316-1370dup
XM_011545732.1:c.253-1370dup (ACSM1)	XP_011544034.1:n.253-1370dup
XR_243258.1:n.960-1370dup (ACSM1)
XR_429672.1:n.960-1370dup (ACSM1)
XR_950737.1:n.960-1370dup (ACSM1)
XR_950738.1:n.960-1370dup (ACSM1)
XR_950740.1:n.960-1370dup (ACSM1)
NM_001318890.1:c.913-1370dup (ACSM1)	NP_001305819.1:n.913-1370dup
NR_134918.1:n.1042-1370dup (ACSM1)
XM_006721016.3:c.913-1370dup (ACSM1)	XP_006721079.1:n.913-1370dup
XM_006721017.3:c.913-1370dup (ACSM1)	XP_006721080.1:n.913-1370dup
XM_006721018.2:c.253-1370dup (ACSM1)	XP_006721081.1:n.253-1370dup
XM_011545729.3:c.913-1370dup (ACSM1)	XP_011544031.1:n.913-1370dup
XM_011545730.3:c.913-1370dup (ACSM1)	XP_011544032.1:n.913-1370dup
XM_011545731.2:c.316-1370dup (ACSM1)	XP_011544033.1:n.316-1370dup
XM_011545732.2:c.253-1370dup (ACSM1)	XP_011544034.1:n.253-1370dup
XM_017022914.2:c.913-1370dup (ACSM1)	XP_016878403.1:n.913-1370dup
XM_017022915.1:c.199-1370dup (ACSM1)	XP_016878404.1:n.199-1370dup
XM_024450148.1:c.253-1370dup (ACSM1)	XP_024305916.1:n.253-1370dup
XR_001751827.2:n.1072-1370dup (ACSM1)
XR_001751828.2:n.1072-1370dup (ACSM1)
XR_243258.3:n.1072-1370dup (ACSM1)
XR_429672.3:n.1072-1370dup (ACSM1)
XR_950737.3:n.1072-1370dup (ACSM1)
XR_950738.3:n.1072-1370dup (ACSM1)
NM_052956.3:c.913-1370dup (ACSM1)	NP_443188.2:n.913-1370dup
NM_001318890.3:c.913-1370dup (ACSM1) MANE Select	NP_001305819.1:n.913-1370dup
NR_134918.2:n.1042-1370dup (ACSM1)