Canonical Allele Identifier: CA407006800
Gene: ACP4 HGNC NCBI
SMIM47 HGNC NCBI

Linked Data

gnomAD v4: 19-50791714-C-T
MyVariant Identifiers: chr19:g.51294971C>T (hg19) chr19:g.50791714C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50791714C>T , CM000681.2:g.50791714C>T GRCh38
NC_000019.9:g.51294971C>T , CM000681.1:g.51294971C>T GRCh37
NC_000019.8:g.55986783C>T NCBI36
NG_052652.1:g.6300C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000270593.2:c.362C>T (ACP4) MANE Select ENSP00000270593.1:p.Ala121Val
ENST00000636757.1:c.-60+691G>A (SMIM47) ENSP00000489695.1:n.-60+691G>A
ENST00000270593.1:c.362C>T (ACP4) ENSP00000270593.1:p.Ala121Val
NM_033068.2:c.362C>T (ACP4) NP_149059.1:p.Ala121Val
XR_936026.1:n.424+691G>A
XR_936026.2:n.434+691G>A
NM_033068.3:c.362C>T (ACP4) MANE Select NP_149059.1:p.Ala121Val
Search 100 bp 5'
Search 100 bp 3'