Canonical Allele Identifier: CA2693442167
Gene: OTC HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367189G>T , CM000685.2:g.38367189G>T GRCh38
NC_000023.10:g.38226442G>T , CM000685.1:g.38226442G>T GRCh37
NC_000023.9:g.38111386G>T NCBI36
NG_008471.1:g.19707G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.78-102G>T MANE Select ENSP00000039007.4:n.78-102G>T
ENST00000643344.1:c.78-102G>T ENSP00000496606.1:n.78-102G>T
ENST00000039007.4:c.78-102G>T ENSP00000039007.4:n.78-102G>T
ENST00000465127.1:c.172-298932G>T ENSP00000417050.1:n.172-298932G>T
ENST00000488812.1:n.170-102G>T
NM_000531.5:c.78-102G>T NP_000522.3:n.78-102G>T
XM_017029556.1:c.78-102G>T XP_016885045.1:n.78-102G>T
NM_000531.6:c.78-102G>T MANE Select NP_000522.3:n.78-102G>T