Canonical Allele Identifier: CA2619249573

Gene: SUOX

Linked Data

• gnomAD v4: 12-56001421-G-GTC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56001421_56001422insTC , CM000674.2:g.56001421_56001422insTC	GRCh38
NC_000012.11:g.56395205_56395206insTC , CM000674.1:g.56395205_56395206insTC	GRCh37
NC_000012.10:g.54681472_54681473insTC	NCBI36
NG_008136.1:g.9163_9164insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266971.8:c.-10-791_-10-790insTC MANE Select	ENSP00000266971.3:n.-10-791_-10-790insTC
ENST00000266971.7:c.-10-791_-10-790insTC	ENSP00000266971.3:n.-10-791_-10-790insTC
ENST00000356124.8:c.-10-791_-10-790insTC	ENSP00000348440.4:n.-10-791_-10-790insTC
ENST00000394115.6:c.-10-791_-10-790insTC	ENSP00000377674.2:n.-10-791_-10-790insTC
ENST00000546833.5:c.-73-465_-73-464insTC	ENSP00000449872.1:n.-73-465_-73-464insTC
ENST00000547586.5:c.-10-791_-10-790insTC	ENSP00000448637.1:n.-10-791_-10-790insTC
ENST00000548274.5:c.-62_-61insTC	ENSP00000450245.1:n.-62_-61insTC
ENST00000550121.5:n.449-386_449-385insTC
ENST00000550340.5:n.54-791_54-790insTC
ENST00000550478.5:n.131-791_131-790insTC
ENST00000551698.5:n.191-791_191-790insTC
ENST00000551841.6:c.-10-791_-10-790insTC	ENSP00000449443.1:n.-10-791_-10-790insTC
ENST00000552258.5:c.-10-791_-10-790insTC	ENSP00000450049.1:n.-10-791_-10-790insTC
ENST00000552363.5:n.82-2197_82-2196insTC
ENST00000552813.5:n.132-791_132-790insTC
NM_000456.2:c.-10-791_-10-790insTC	NP_000447.2:n.-10-791_-10-790insTC
NM_001032386.1:c.-10-791_-10-790insTC	NP_001027558.1:n.-10-791_-10-790insTC
NM_001032387.1:c.-10-791_-10-790insTC	NP_001027559.1:n.-10-791_-10-790insTC
XM_005269112.1:c.-52-465_-52-464insTC	XP_005269169.1:n.-52-465_-52-464insTC
XM_017019905.2:c.-52-465_-52-464insTC	XP_016875394.1:n.-52-465_-52-464insTC
XM_017019906.1:c.-52-465_-52-464insTC	XP_016875395.1:n.-52-465_-52-464insTC
XM_017019907.2:c.-10-791_-10-790insTC	XP_016875396.1:n.-10-791_-10-790insTC
XM_017019908.1:c.-11+699_-11+700insTC	XP_016875397.1:n.-11+699_-11+700insTC
XM_024449167.1:c.-52-465_-52-464insTC	XP_024304935.1:n.-52-465_-52-464insTC
NM_001032386.2:c.-10-791_-10-790insTC MANE Select	NP_001027558.1:n.-10-791_-10-790insTC
NM_000456.3:c.-10-791_-10-790insTC	NP_000447.2:n.-10-791_-10-790insTC
NM_001032387.2:c.-10-791_-10-790insTC	NP_001027559.1:n.-10-791_-10-790insTC