Canonical Allele Identifier: CA2424870763
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367190_38367194delinsAAAAG , CM000685.2:g.38367190_38367194delinsAAAAG GRCh38
NC_000023.10:g.38226443_38226447delinsAAAAG , CM000685.1:g.38226443_38226447delinsAAAAG GRCh37
NC_000023.9:g.38111387_38111391delinsAAAAG NCBI36
NG_008471.1:g.19708_19712delinsAAAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.78-101_78-97delinsAAAAG MANE Select ENSP00000039007.4:n.78-101_78-97delinsAAA...
ENST00000643344.1:c.78-101_78-97delinsAAAAG ENSP00000496606.1:n.78-101_78-97delinsAAA...
ENST00000039007.4:c.78-101_78-97delinsAAAAG ENSP00000039007.4:n.78-101_78-97delinsAAA...
ENST00000465127.1:c.172-298931_172-298927delinsAAAAG ENSP00000417050.1:n.172-298931_172-298927...
ENST00000488812.1:n.170-101_170-97delinsAAAAG
NM_000531.5:c.78-101_78-97delinsAAAAG NP_000522.3:n.78-101_78-97delinsAAAAG
XM_017029556.1:c.78-101_78-97delinsAAAAG XP_016885045.1:n.78-101_78-97delinsAAAAG
NM_000531.6:c.78-101_78-97delinsAAAAG MANE Select NP_000522.3:n.78-101_78-97delinsAAAAG