Canonical Allele Identifier: CA3168151

Gene: TRIML2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.188097124G>A , CM000666.2:g.188097124G>A	GRCh38
NC_000004.11:g.189018278G>A , CM000666.1:g.189018278G>A	GRCh37
NC_000004.10:g.189255272G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_173553.4:c.682C>T MANE Select	NP_775824.2:p.His228Tyr
ENST00000682553.1:c.682C>T MANE Select	ENSP00000507413.1:p.His228Tyr
NM_001303419.1:c.757C>T	NP_001290348.1:p.His253Tyr
NM_173553.2:c.682C>T	NP_775824.2:p.His228Tyr
NM_173553.3:c.682C>T	NP_775824.2:p.His228Tyr
ENST00000326754.7:c.637C>T	ENSP00000317498.4:p.His213Tyr
ENST00000503141.1:c.374C>T	ENSP00000426074.1:n.374C>T
ENST00000503475.5:c.374C>T	ENSP00000421575.1:n.374C>T
ENST00000512729.5:c.682C>T	ENSP00000422581.2:p.His228Tyr
XM_011531737.1:c.682C>T	XP_011530039.1:p.His228Tyr
XM_011531737.2:c.682C>T	XP_011530039.1:p.His228Tyr
XM_011531738.1:c.682C>T	XP_011530040.1:p.His228Tyr
XM_011531738.2:c.682C>T	XP_011530040.1:p.His228Tyr
XM_011531739.1:c.406C>T	XP_011530041.1:p.His136Tyr
XR_938703.1:n.1205C>T
XR_938703.2:n.1207C>T
XR_938704.1:n.1182C>T
XR_938704.2:n.1184C>T
XR_938705.1:n.1182C>T
XR_938705.2:n.1184C>T