Canonical Allele Identifier: CA515650711

Gene: OTC

Linked Data

• MyVariant Identifiers: chrX:g.38262966A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38403713A>G , CM000685.2:g.38403713A>G	GRCh38
NC_000023.10:g.38262966A>G , CM000685.1:g.38262966A>G	GRCh37
NC_000023.9:g.38147910A>G	NCBI36
NG_008471.1:g.56231A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.636A>G MANE Select	ENSP00000039007.4:p.Gly212=
ENST00000643344.1:c.*386A>G	ENSP00000496606.1:n.*386A>G
ENST00000039007.4:c.636A>G	ENSP00000039007.4:p.Gly212=
ENST00000465127.1:c.172-262408A>G	ENSP00000417050.1:n.172-262408A>G
NM_000531.5:c.636A>G	NP_000522.3:p.Gly212=
XM_017029556.1:c.636A>G	XP_016885045.1:p.Gly212=
NM_000531.6:c.636A>G MANE Select	NP_000522.3:p.Gly212=