Canonical Allele Identifier: CA2624689783

Gene: TOGARAM1

Linked Data

• gnomAD v4: 14-45073876-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073876G>C , CM000676.2:g.45073876G>C	GRCh38
NC_000014.8:g.45543079G>C , CM000676.1:g.45543079G>C	GRCh37
NC_000014.7:g.44612829G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*315G>C MANE Select	ENSP00000354917.2:n.*315G>C
ENST00000361462.6:c.*315G>C	ENSP00000354917.2:n.*315G>C
ENST00000361577.7:c.*315G>C	ENSP00000355045.3:n.*315G>C
ENST00000557423.5:c.*2480G>C	ENSP00000451829.1:n.*2480G>C
NM_001308120.1:c.*315G>C	NP_001295049.1:n.*315G>C
NM_015091.2:c.*315G>C	NP_055906.2:n.*315G>C
NM_015091.3:c.*315G>C	NP_055906.2:n.*315G>C
NR_131765.1:n.5700G>C
XM_011536571.1:c.*620G>C	XP_011534873.1:n.*620G>C
XM_017021098.1:c.*315G>C	XP_016876587.1:n.*315G>C
XM_017021099.1:c.*315G>C	XP_016876588.1:n.*315G>C
XR_001750194.1:n.5964G>C
XR_001750195.1:n.5607G>C
NM_001308120.2:c.*315G>C MANE Select	NP_001295049.1:n.*315G>C
NM_015091.4:c.*315G>C	NP_055906.2:n.*315G>C
NR_131765.2:n.5700G>C