Canonical Allele Identifier: CA640863209
Gene: OTC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367288C>T , CM000685.2:g.38367288C>T GRCh38
NC_000023.10:g.38226541C>T , CM000685.1:g.38226541C>T GRCh37
NC_000023.9:g.38111485C>T NCBI36
NG_008471.1:g.19806C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.78-3C>T MANE Select ENSP00000039007.4:n.78-3C>T
ENST00000643344.1:c.78-3C>T ENSP00000496606.1:n.78-3C>T
ENST00000039007.4:c.78-3C>T ENSP00000039007.4:n.78-3C>T
ENST00000465127.1:c.172-298833C>T ENSP00000417050.1:n.172-298833C>T
ENST00000488812.1:n.170-3C>T
NM_000531.5:c.78-3C>T NP_000522.3:n.78-3C>T
XM_017029556.1:c.78-3C>T XP_016885045.1:n.78-3C>T
NM_000531.6:c.78-3C>T MANE Select NP_000522.3:n.78-3C>T