Canonical Allele Identifier: CA2424870759

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38367184_38367189delinsAAAAAG , CM000685.2:g.38367184_38367189delinsAAAAAG	GRCh38
NC_000023.10:g.38226437_38226442delinsAAAAAG , CM000685.1:g.38226437_38226442delinsAAAAAG	GRCh37
NC_000023.9:g.38111381_38111386delinsAAAAAG	NCBI36
NG_008471.1:g.19702_19707delinsAAAAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000039007.5:c.78-107_78-102delinsAAAAAG MANE Select	ENSP00000039007.4:n.78-107_78-102delinsAA...
ENST00000643344.1:c.78-107_78-102delinsAAAAAG	ENSP00000496606.1:n.78-107_78-102delinsAA...
ENST00000039007.4:c.78-107_78-102delinsAAAAAG	ENSP00000039007.4:n.78-107_78-102delinsAA...
ENST00000465127.1:c.172-298937_172-298932delinsAAAAAG	ENSP00000417050.1:n.172-298937_172-298932...
ENST00000488812.1:n.170-107_170-102delinsAAAAAG
NM_000531.5:c.78-107_78-102delinsAAAAAG	NP_000522.3:n.78-107_78-102delinsAAAAAG
XM_017029556.1:c.78-107_78-102delinsAAAAAG	XP_016885045.1:n.78-107_78-102delinsAAAAA...
NM_000531.6:c.78-107_78-102delinsAAAAAG MANE Select	NP_000522.3:n.78-107_78-102delinsAAAAAG