Canonical Allele Identifier: CA378685874

Gene: UROS

Linked Data

• gnomAD v4: 10-125788980-G-T
• MyVariant Identifiers: chr10:g.127477549G>T (hg19) ; chr10:g.125788980G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125788980G>T , CM000672.2:g.125788980G>T	GRCh38
NC_000010.10:g.127477549G>T , CM000672.1:g.127477549G>T	GRCh37
NC_000010.9:g.127467539G>T	NCBI36
NG_011557.1:g.39289C>A
NG_011557.2:g.39289C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.686C>A	ENSP00000518871.1:p.Ala229Asp
ENST00000368797.10:c.686C>A MANE Select	ENSP00000357787.4:p.Ala229Asp
ENST00000465577.6:c.706C>A
ENST00000648427.1:c.*684C>A	ENSP00000497909.1:n.*684C>A
ENST00000649536.1:c.686C>A	ENSP00000497817.1:p.Ala229Asp
ENST00000650185.1:c.836C>A
ENST00000650472.1:n.3072C>A
ENST00000650524.1:c.599C>A	ENSP00000498108.1:n.599C>A
ENST00000650587.1:c.767C>A	ENSP00000497366.1:p.Ala256Asp
ENST00000368786.5:c.686C>A	ENSP00000357775.1:p.Ala229Asp
ENST00000368797.8:c.686C>A	ENSP00000357787.4:p.Ala229Asp
ENST00000464267.1:n.783C>A
ENST00000465577.5:n.328C>A
ENST00000470483.1:n.374C>A
ENST00000484541.5:n.459C>A
ENST00000616800.4:c.161-3720C>A
ENST00000622016.4:c.241-3141C>A	ENSP00000483041.1:n.241-3141C>A
NM_000375.2:c.686C>A	NP_000366.1:p.Ala229Asp
XM_005270137.2:c.767C>A	XP_005270194.1:p.Ala256Asp
XM_005270138.2:c.686C>A	XP_005270195.1:p.Ala229Asp
XM_005270139.2:c.661-3141C>A	XP_005270196.1:n.661-3141C>A
XM_006717960.2:c.767C>A	XP_006718023.1:p.Ala256Asp
XM_011540127.1:c.661-3720C>A	XP_011538429.1:n.661-3720C>A
XR_246103.2:n.866C>A
XR_945810.1:n.1096C>A
NM_000375.3:c.686C>A MANE Select	NP_000366.1:p.Ala229Asp
NM_001324036.1:c.767C>A	NP_001310965.1:p.Ala256Asp
NM_001324037.1:c.686C>A	NP_001310966.1:p.Ala229Asp
NM_001324038.1:c.605C>A	NP_001310967.1:p.Ala202Asp
NR_136675.1:n.771C>A
NR_136676.1:n.1198C>A
NR_136677.1:n.927-3141C>A
NR_136678.1:n.682C>A
XM_011540127.2:c.661-3720C>A	XP_011538429.1:n.661-3720C>A
XM_017016611.2:c.767C>A	XP_016872100.2:p.Ala256Asp
XM_017016612.2:c.661-3141C>A	XP_016872101.1:n.661-3141C>A
XM_024448154.1:c.686C>A	XP_024303922.1:p.Ala229Asp
XR_002957010.1:n.2025C>A
XR_246103.3:n.881C>A
XR_945810.2:n.1111C>A
NM_001324036.2:c.767C>A	NP_001310965.1:p.Ala256Asp
NM_001324037.2:c.686C>A	NP_001310966.1:p.Ala229Asp
NM_001324038.2:c.605C>A	NP_001310967.1:p.Ala202Asp
NR_136675.2:n.761C>A
NR_136676.2:n.1188C>A
NR_136678.2:n.672C>A
NR_136677.2:n.917-3141C>A