Canonical Allele Identifier: CA2693443317
Gene: OTC HGNC NCBI

Linked Data

gnomAD v4: X-38369712-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369712C>T , CM000685.2:g.38369712C>T GRCh38
NC_000023.10:g.38228965C>T , CM000685.1:g.38228965C>T GRCh37
NC_000023.9:g.38113909C>T NCBI36
NG_008471.1:g.22230C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.217-84C>T MANE Select ENSP00000039007.4:n.217-84C>T
ENST00000643344.1:c.217-84C>T ENSP00000496606.1:n.217-84C>T
ENST00000039007.4:c.217-84C>T ENSP00000039007.4:n.217-84C>T
ENST00000465127.1:c.172-296409C>T ENSP00000417050.1:n.172-296409C>T
ENST00000488812.1:n.309-84C>T
NM_000531.5:c.217-84C>T NP_000522.3:n.217-84C>T
XM_017029556.1:c.217-84C>T XP_016885045.1:n.217-84C>T
NM_000531.6:c.217-84C>T MANE Select NP_000522.3:n.217-84C>T
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