Canonical Allele Identifier: CA2424870751

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38367173_38367177delinsTCAAA , CM000685.2:g.38367173_38367177delinsTCAAA	GRCh38
NC_000023.10:g.38226426_38226430delinsTCAAA , CM000685.1:g.38226426_38226430delinsTCAAA	GRCh37
NC_000023.9:g.38111370_38111374delinsTCAAA	NCBI36
NG_008471.1:g.19691_19695delinsTCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.78-118_78-114delinsTCAAA MANE Select	ENSP00000039007.4:n.78-118_78-114delinsTCAAA
ENST00000643344.1:c.78-118_78-114delinsTCAAA	ENSP00000496606.1:n.78-118_78-114delinsTCAAA
ENST00000039007.4:c.78-118_78-114delinsTCAAA	ENSP00000039007.4:n.78-118_78-114delinsTCAAA
ENST00000465127.1:c.172-298948_172-298944delinsTCAAA	ENSP00000417050.1:n.172-298948_172-298944delinsTCAAA
ENST00000488812.1:n.170-118_170-114delinsTCAAA
NM_000531.5:c.78-118_78-114delinsTCAAA	NP_000522.3:n.78-118_78-114delinsTCAAA
XM_017029556.1:c.78-118_78-114delinsTCAAA	XP_016885045.1:n.78-118_78-114delinsTCAAA
NM_000531.6:c.78-118_78-114delinsTCAAA MANE Select	NP_000522.3:n.78-118_78-114delinsTCAAA