Canonical Allele Identifier: CA327944365

Gene: OTC

Linked Data

• dbSNP Id: rs1555975895
• MyVariant Identifiers: chrX:g.38262701_38262702insATC (hg19) ; chrX:g.38403448_38403449insATC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38403448_38403449insATC , CM000685.2:g.38403448_38403449insATC	GRCh38
NC_000023.10:g.38262701_38262702insATC , CM000685.1:g.38262701_38262702insATC	GRCh37
NC_000023.9:g.38147645_38147646insATC	NCBI36
NG_008471.1:g.55966_55967insATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.541-170_541-169insATC MANE Select	ENSP00000039007.4:n.541-170_541-169insATC
ENST00000643344.1:c.*291-170_*291-169insATC	ENSP00000496606.1:n.*291-170_*291-169insATC
ENST00000039007.4:c.541-170_541-169insATC	ENSP00000039007.4:n.541-170_541-169insATC
ENST00000465127.1:c.172-262673_172-262672insATC	ENSP00000417050.1:n.172-262673_172-262672insATC
ENST00000488812.1:n.578-170_578-169insATC
NM_000531.5:c.541-170_541-169insATC	NP_000522.3:n.541-170_541-169insATC
XM_017029556.1:c.541-170_541-169insATC	XP_016885045.1:n.541-170_541-169insATC
NM_000531.6:c.541-170_541-169insATC MANE Select	NP_000522.3:n.541-170_541-169insATC