Canonical Allele Identifier: CA1290396208

Gene: ACMSD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.134842216C= , CM000664.2:g.134842216C=	GRCh38
NC_000002.11:g.135599786C= , CM000664.1:g.135599786C=	GRCh37
NC_000002.10:g.135316256C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356140.10:c.58-3017C= MANE Select	ENSP00000348459.5:n.58-3017C=
ENST00000356140.9:c.58-3017C=	ENSP00000348459.5:n.58-3017C=
ENST00000392928.5:c.-174-2149C=	ENSP00000376659.1:n.-174-2149C=
ENST00000485893.5:n.125-3017C=
NM_001307983.1:c.-174-2149C=	NP_001294912.1:n.-174-2149C=
NM_138326.2:c.58-3017C=	NP_612199.2:n.58-3017C=
XM_005263586.3:c.58-3017C=	XP_005263643.1:n.58-3017C=
XM_005263588.3:c.-67-3017C=	XP_005263645.1:n.-67-3017C=
XM_005263589.3:c.-242-2143C=	XP_005263646.1:n.-242-2143C=
XM_011510592.1:c.-180-2143C=	XP_011508894.1:n.-180-2143C=
XM_005263586.4:c.58-3017C=	XP_005263643.1:n.58-3017C=
XM_005263588.4:c.-67-3017C=	XP_005263645.1:n.-67-3017C=
XM_005263589.4:c.-242-2143C=	XP_005263646.1:n.-242-2143C=
XM_011510592.2:c.-180-2143C=	XP_011508894.1:n.-180-2143C=
XM_017003325.1:c.-177-2146C=	XP_016858814.1:n.-177-2146C=
XM_024452690.1:c.-239-2146C=	XP_024308458.1:n.-239-2146C=
XM_024452691.1:c.-236-2149C=	XP_024308459.1:n.-236-2149C=
NM_138326.3:c.58-3017C= MANE Select	NP_612199.2:n.58-3017C=
NM_001307983.2:c.-174-2149C=	NP_001294912.1:n.-174-2149C=