Canonical Allele Identifier: CA2693442232

Gene: OTC

Linked Data

• gnomAD v4: X-38367270-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38367270C>T , CM000685.2:g.38367270C>T	GRCh38
NC_000023.10:g.38226523C>T , CM000685.1:g.38226523C>T	GRCh37
NC_000023.9:g.38111467C>T	NCBI36
NG_008471.1:g.19788C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000039007.5:c.78-21C>T MANE Select	ENSP00000039007.4:n.78-21C>T
ENST00000643344.1:c.78-21C>T	ENSP00000496606.1:n.78-21C>T
ENST00000039007.4:c.78-21C>T	ENSP00000039007.4:n.78-21C>T
ENST00000465127.1:c.172-298851C>T	ENSP00000417050.1:n.172-298851C>T
ENST00000488812.1:n.170-21C>T
NM_000531.5:c.78-21C>T	NP_000522.3:n.78-21C>T
XM_017029556.1:c.78-21C>T	XP_016885045.1:n.78-21C>T
NM_000531.6:c.78-21C>T MANE Select	NP_000522.3:n.78-21C>T