Canonical Allele Identifier: CA31366329

Gene: FCER1A

Linked Data

• dbSNP Id: rs1002000887
• MyVariant Identifiers: chr1:g.159273900G>A (hg19) ; chr1:g.159304110G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159304110G>A , CM000663.2:g.159304110G>A	GRCh38
NC_000001.10:g.159273900G>A , CM000663.1:g.159273900G>A	GRCh37
NC_000001.9:g.157540524G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000693622.1:c.259G>A MANE Select	ENSP00000509626.1:p.Asp87Asn
ENST00000368114.1:c.160G>A	ENSP00000357096.1:p.Asp54Asn
ENST00000368115.5:c.259G>A	ENSP00000357097.1:p.Asp87Asn
NM_002001.3:c.259G>A	NP_001992.1:p.Asp87Asn
NM_001387280.1:c.259G>A MANE Select	NP_001374209.1:p.Asp87Asn
NM_001387281.1:c.76+1236G>A	NP_001374210.1:n.76+1236G>A
NM_001387282.1:c.160G>A	NP_001374211.1:p.Asp54Asn
NM_002001.4:c.259G>A	NP_001992.1:p.Asp87Asn