Canonical Allele Identifier: CA748040

Gene: TRIM62 AZIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.33159731C>T , CM000663.2:g.33159731C>T	GRCh38
NC_000001.10:g.33625332C>T , CM000663.1:g.33625332C>T	GRCh37
NC_000001.9:g.33397919C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291416.10:c.718G>A (TRIM62) MANE Select	ENSP00000291416.5:p.Asp240Asn
ENST00000291416.9:c.718G>A (TRIM62)	ENSP00000291416.5:p.Asp240Asn
ENST00000485148.1:n.767G>A (TRIM62)
ENST00000543586.1:c.355G>A (TRIM62)	ENSP00000441173.1:p.Asp119Asn
NM_018207.2:c.718G>A (TRIM62)	NP_060677.2:p.Asp240Asn
XM_011540558.1:c.1030-1121C>T (AZIN2)	XP_011538860.1:n.1030-1121C>T
XM_011540559.1:c.1030-1121C>T (AZIN2)	XP_011538861.1:n.1030-1121C>T
XM_011540560.1:c.1030-1121C>T (AZIN2)	XP_011538862.1:n.1030-1121C>T
XM_011540561.1:c.1030-1121C>T (AZIN2)	XP_011538863.1:n.1030-1121C>T
XM_011540562.1:c.1030-1121C>T (AZIN2)	XP_011538864.1:n.1030-1121C>T
XM_011540565.1:c.1041-1121C>T (AZIN2)	XP_011538867.1:n.1041-1121C>T
XM_011541705.1:c.355G>A (TRIM62)	XP_011540007.1:p.Asp119Asn
NM_001330483.1:c.355G>A (TRIM62)	NP_001317412.1:p.Asp119Asn
XM_017000167.1:c.1030-1121C>T (AZIN2)	XP_016855656.1:n.1030-1121C>T
XM_017000174.1:c.1041-1121C>T (AZIN2)	XP_016855663.1:n.1041-1121C>T
XM_017001629.2:c.958G>A (TRIM62)	XP_016857118.1:p.Asp320Asn
XM_017001630.1:c.925G>A (TRIM62)	XP_016857119.1:p.Asp309Asn
NM_018207.3:c.718G>A (TRIM62) MANE Select	NP_060677.2:p.Asp240Asn
NM_001330483.2:c.355G>A (TRIM62)	NP_001317412.1:p.Asp119Asn