Canonical Allele Identifier: CA2147319575
Community Standard Title: NM_001107.5(ACYP1):c.*82A=
Gene: ACYP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75053362T= , CM000676.2:g.75053362T= GRCh38
NC_000014.8:g.75520065T= , CM000676.1:g.75520065T= GRCh37
NC_000014.7:g.74589818T= NCBI36
NG_008649.1:g.3171A= , LRG_217:g.3171A=

Transcript Alleles

HGVS Amino-acid Change
NM_001107.5:c.*82A= MANE Select NP_001098.1:n.*82A=
ENST00000238618.8:c.*82A= MANE Select ENSP00000238618.3:n.*82A=
NM_001107.4:c.*82A= NP_001098.1:n.*82A=
NM_001302616.1:c.*82A= NP_001289545.1:n.*82A=
NM_001302616.2:c.*82A= NP_001289545.1:n.*82A=
NM_001302617.1:c.*82A= NP_001289546.1:n.*82A=
NM_001302617.2:c.*82A= NP_001289546.1:n.*82A=
NR_126393.1:n.565A=
NR_126393.2:n.540A=
NR_126394.1:n.572A=
NR_126394.2:n.579A=
NR_126395.1:n.394A=
NR_126395.2:n.369A=
ENST00000238618.7:c.*82A= ENSP00000238618.3:n.*82A=
ENST00000357971.7:c.*293A= ENSP00000350655.3:n.*293A=
ENST00000555463.1:c.*82A= ENSP00000450873.1:n.*82A=
ENST00000555694.5:c.*82A= ENSP00000451581.1:n.*82A=