Canonical Allele Identifier: CA327944699

Gene: OTC

Linked Data

• dbSNP Id: rs775409646
• gnomAD v4: X-38403772-C-T
• MyVariant Identifiers: chrX:g.38263025C>T (hg19) ; chrX:g.38403772C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38403772C>T , CM000685.2:g.38403772C>T	GRCh38
NC_000023.10:g.38263025C>T , CM000685.1:g.38263025C>T	GRCh37
NC_000023.9:g.38147969C>T	NCBI36
NG_008471.1:g.56290C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.663+32C>T MANE Select	ENSP00000039007.4:n.663+32C>T
ENST00000643344.1:c.*413+32C>T	ENSP00000496606.1:n.*413+32C>T
ENST00000039007.4:c.663+32C>T	ENSP00000039007.4:n.663+32C>T
ENST00000465127.1:c.172-262349C>T	ENSP00000417050.1:n.172-262349C>T
NM_000531.5:c.663+32C>T	NP_000522.3:n.663+32C>T
XM_017029556.1:c.663+32C>T	XP_016885045.1:n.663+32C>T
NM_000531.6:c.663+32C>T MANE Select	NP_000522.3:n.663+32C>T