Canonical Allele Identifier: CA1290396275
Gene: ACMSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.134842373G= , CM000664.2:g.134842373G= GRCh38
NC_000002.11:g.135599943G= , CM000664.1:g.135599943G= GRCh37
NC_000002.10:g.135316413G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356140.10:c.58-2860G= MANE Select ENSP00000348459.5:n.58-2860G=
ENST00000356140.9:c.58-2860G= ENSP00000348459.5:n.58-2860G=
ENST00000392928.5:c.-174-1992G= ENSP00000376659.1:n.-174-1992G=
ENST00000485893.5:n.125-2860G=
NM_001307983.1:c.-174-1992G= NP_001294912.1:n.-174-1992G=
NM_138326.2:c.58-2860G= NP_612199.2:n.58-2860G=
XM_005263586.3:c.58-2860G= XP_005263643.1:n.58-2860G=
XM_005263588.3:c.-67-2860G= XP_005263645.1:n.-67-2860G=
XM_005263589.3:c.-242-1986G= XP_005263646.1:n.-242-1986G=
XM_011510592.1:c.-180-1986G= XP_011508894.1:n.-180-1986G=
XM_005263586.4:c.58-2860G= XP_005263643.1:n.58-2860G=
XM_005263588.4:c.-67-2860G= XP_005263645.1:n.-67-2860G=
XM_005263589.4:c.-242-1986G= XP_005263646.1:n.-242-1986G=
XM_011510592.2:c.-180-1986G= XP_011508894.1:n.-180-1986G=
XM_017003325.1:c.-177-1989G= XP_016858814.1:n.-177-1989G=
XM_017003326.1:c.-1161G= XP_016858815.1:n.-1161G=
XM_024452690.1:c.-239-1989G= XP_024308458.1:n.-239-1989G=
XM_024452691.1:c.-236-1992G= XP_024308459.1:n.-236-1992G=
NM_138326.3:c.58-2860G= MANE Select NP_612199.2:n.58-2860G=
NM_001307983.2:c.-174-1992G= NP_001294912.1:n.-174-1992G=