Canonical Allele Identifier: CA15803760
Gene: ACYP1 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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