Canonical Allele Identifier: CA2693443332
Gene: OTC HGNC NCBI

Linked Data

gnomAD v4: X-38369734-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369734G>T , CM000685.2:g.38369734G>T GRCh38
NC_000023.10:g.38228987G>T , CM000685.1:g.38228987G>T GRCh37
NC_000023.9:g.38113931G>T NCBI36
NG_008471.1:g.22252G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.217-62G>T MANE Select ENSP00000039007.4:n.217-62G>T
ENST00000643344.1:c.217-62G>T ENSP00000496606.1:n.217-62G>T
ENST00000039007.4:c.217-62G>T ENSP00000039007.4:n.217-62G>T
ENST00000465127.1:c.172-296387G>T ENSP00000417050.1:n.172-296387G>T
ENST00000488812.1:n.309-62G>T
NM_000531.5:c.217-62G>T NP_000522.3:n.217-62G>T
XM_017029556.1:c.217-62G>T XP_016885045.1:n.217-62G>T
NM_000531.6:c.217-62G>T MANE Select NP_000522.3:n.217-62G>T
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