Canonical Allele Identifier: CA4985461
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 374020
dbSNP Id: rs771055145
gnomAD v2: 9-12704577-A-G
gnomAD v3: 9-12704577-A-G
gnomAD v4: 9-12704577-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12704577A>G , CM000671.2:g.12704577A>G GRCh38
NC_000009.11:g.12704577A>G , CM000671.1:g.12704577A>G GRCh37
NC_000009.10:g.12694577A>G NCBI36
NG_011705.1:g.16192A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.1133A>G (TYRP1) MANE Select ENSP00000373570.4:p.Asn378Ser
ENST00000381136.2:c.263A>G (TYRP1) ENSP00000370528.2:p.Asn88Ser
ENST00000381142.3:n.370A>G (TYRP1)
ENST00000388918.9:c.1133A>G (TYRP1) ENSP00000373570.4:p.Asn378Ser
NM_000550.2:c.1133A>G (TYRP1) NP_000541.1:p.Asn378Ser
NR_125775.1:n.317-3951T>C (LURAP1L-AS1)
XR_001746372.2:n.1117A>G (TYRP1)
NM_000550.3:c.1133A>G (TYRP1) MANE Select NP_000541.1:p.Asn378Ser