Canonical Allele Identifier: CA2579584828

Gene: OTC

Linked Data

• gnomAD v4: X-38403551-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38403553del , CM000685.2:g.38403553del	GRCh38
NC_000023.10:g.38262806del , CM000685.1:g.38262806del	GRCh37
NC_000023.9:g.38147750del	NCBI36
NG_008471.1:g.56071del

Transcript Alleles

HGVS	Amino-acid change
ENST00000039007.5:c.541-65del MANE Select	ENSP00000039007.4:n.541-65del
ENST00000643344.1:c.*291-65del	ENSP00000496606.1:n.*291-65del
ENST00000039007.4:c.541-65del	ENSP00000039007.4:n.541-65del
ENST00000465127.1:c.172-262568del	ENSP00000417050.1:n.172-262568del
ENST00000488812.1:n.578-65del
NM_000531.5:c.541-65del	NP_000522.3:n.541-65del
XM_017029556.1:c.541-65del	XP_016885045.1:n.541-65del
NM_000531.6:c.541-65del MANE Select	NP_000522.3:n.541-65del