Canonical Allele Identifier: CA508201018
Gene: ACP4 HGNC NCBI
SMIM47 HGNC NCBI

Linked Data

dbSNP Id: rs1449685112
gnomAD v2: 19-51295026-C-A
gnomAD v4: 19-50791769-C-A
MyVariant Identifiers: chr19:g.51295026C>A (hg19) chr19:g.50791769C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50791769C>A , CM000681.2:g.50791769C>A GRCh38
NC_000019.9:g.51295026C>A , CM000681.1:g.51295026C>A GRCh37
NC_000019.8:g.55986838C>A NCBI36
NG_052652.1:g.6355C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270593.2:c.417C>A (ACP4) MANE Select ENSP00000270593.1:p.Ile139=
ENST00000636757.1:c.-60+636G>T (SMIM47) ENSP00000489695.1:n.-60+636G>T
ENST00000270593.1:c.417C>A (ACP4) ENSP00000270593.1:p.Ile139=
NM_033068.2:c.417C>A (ACP4) NP_149059.1:p.Ile139=
XR_936026.1:n.424+636G>T
XR_936026.2:n.434+636G>T
NM_033068.3:c.417C>A (ACP4) MANE Select NP_149059.1:p.Ile139=
Search 100 bp 5'
Search 100 bp 3'