Canonical Allele Identifier: CA7167012

Gene: TOGARAM1 KLHL28

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44963533C>A , CM000676.2:g.44963533C>A	GRCh38
NC_000014.8:g.45432736C>A , CM000676.1:g.45432736C>A	GRCh37
NC_000014.7:g.44502486C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001308120.2:c.1112C>A (TOGARAM1) MANE Select	NP_001295049.1:p.Ala371Asp
ENST00000361462.7:c.1112C>A (TOGARAM1) MANE Select	ENSP00000354917.2:p.Ala371Asp
NM_001308120.1:c.1112C>A (TOGARAM1)	NP_001295049.1:p.Ala371Asp
NM_015091.2:c.1112C>A (TOGARAM1)	NP_055906.2:p.Ala371Asp
NM_015091.3:c.1112C>A (TOGARAM1)	NP_055906.2:p.Ala371Asp
NM_015091.4:c.1112C>A (TOGARAM1)	NP_055906.2:p.Ala371Asp
NR_131765.1:n.1344C>A (TOGARAM1)
NR_131765.2:n.1344C>A (TOGARAM1)
ENST00000361462.6:c.1112C>A (TOGARAM1)	ENSP00000354917.2:p.Ala371Asp
ENST00000361577.7:c.1112C>A (TOGARAM1)	ENSP00000355045.3:p.Ala371Asp
ENST00000555607.1:n.1320C>A (TOGARAM1)
ENST00000555945.1:n.1315C>A (TOGARAM1)
ENST00000556239.5:c.-1+14665G>T (KLHL28)	ENSP00000452591.1:n.-1+14665G>T
ENST00000557423.5:c.1112C>A (TOGARAM1)	ENSP00000451829.1:p.Ala371Asp
XM_006720083.1:c.1112C>A (TOGARAM1)	XP_006720146.1:p.Ala371Asp
XM_011536571.1:c.1112C>A (TOGARAM1)	XP_011534873.1:p.Ala371Asp
XM_011536572.1:c.1112C>A (TOGARAM1)	XP_011534874.1:p.Ala371Asp
XM_011536573.1:c.1112C>A (TOGARAM1)	XP_011534875.1:p.Ala371Asp
XM_011536848.1:c.-1+14665G>T (KLHL28)	XP_011535150.1:n.-1+14665G>T
XM_017021098.1:c.1112C>A (TOGARAM1)	XP_016876587.1:p.Ala371Asp
XM_017021099.1:c.1112C>A (TOGARAM1)	XP_016876588.1:p.Ala371Asp
XM_017021100.1:c.1112C>A (TOGARAM1)	XP_016876589.1:p.Ala371Asp
XR_001750194.1:n.1315C>A (TOGARAM1)
XR_001750195.1:n.1315C>A (TOGARAM1)
XR_245674.1:n.1315C>A (TOGARAM1)
XR_943403.1:n.1315C>A (TOGARAM1)
XR_943403.2:n.1315C>A (TOGARAM1)
XR_943404.1:n.1315C>A (TOGARAM1)