Canonical Allele Identifier: CA412723062
Gene: OTC HGNC NCBI

Linked Data

dbSNP Id: rs1218297443
gnomAD v2: X-38268211-G-A
gnomAD v3: X-38408958-G-A
gnomAD v4: X-38408958-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38408958G>A , CM000685.2:g.38408958G>A GRCh38
NC_000023.10:g.38268211G>A , CM000685.1:g.38268211G>A GRCh37
NC_000023.9:g.38153155G>A NCBI36
NG_008471.1:g.61476G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.800G>A MANE Select ENSP00000039007.4:p.Ser267Asn
ENST00000643344.1:c.*550G>A ENSP00000496606.1:n.*550G>A
ENST00000039007.4:c.800G>A ENSP00000039007.4:p.Ser267Asn
ENST00000465127.1:c.172-257163G>A ENSP00000417050.1:n.172-257163G>A
NM_000531.5:c.800G>A NP_000522.3:p.Ser267Asn
XM_017029556.1:c.800G>A XP_016885045.1:p.Ser267Asn
NM_000531.6:c.800G>A MANE Select NP_000522.3:p.Ser267Asn