Canonical Allele Identifier: CA2838529223

Gene: TRIML2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.188103823T>C , CM000666.2:g.188103823T>C	GRCh38
NC_000004.11:g.189024977T>C , CM000666.1:g.189024977T>C	GRCh37
NC_000004.10:g.189261971T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682553.1:c.285+1014A>G MANE Select	ENSP00000507413.1:n.285+1014A>G
ENST00000326754.7:c.165+1014A>G	ENSP00000317498.4:n.165+1014A>G
ENST00000511771.1:n.510+1014A>G
ENST00000512729.5:c.285+1014A>G	ENSP00000422581.2:n.285+1014A>G
NM_001303419.1:c.285+1014A>G	NP_001290348.1:n.285+1014A>G
NM_173553.2:c.285+1014A>G	NP_775824.2:n.285+1014A>G
XM_011531737.1:c.285+1014A>G	XP_011530039.1:n.285+1014A>G
XM_011531738.1:c.285+1014A>G	XP_011530040.1:n.285+1014A>G
XM_011531739.1:c.-15+1014A>G	XP_011530041.1:n.-15+1014A>G
XR_938703.1:n.808+1014A>G
XR_938704.1:n.808+1014A>G
XR_938705.1:n.808+1014A>G
NM_173553.3:c.285+1014A>G	NP_775824.2:n.285+1014A>G
XM_011531737.2:c.285+1014A>G	XP_011530039.1:n.285+1014A>G
XM_011531738.2:c.285+1014A>G	XP_011530040.1:n.285+1014A>G
XR_938703.2:n.810+1014A>G
XR_938704.2:n.810+1014A>G
XR_938705.2:n.810+1014A>G
NM_173553.4:c.285+1014A>G MANE Select	NP_775824.2:n.285+1014A>G