Canonical Allele Identifier: CA2830536674

Gene: NSUN7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40807242_40807243insATGA , CM000666.2:g.40807242_40807243insATGA	GRCh38
NC_000004.11:g.40809259_40809260insATGA , CM000666.1:g.40809259_40809260insATGA	GRCh37
NC_000004.10:g.40504016_40504017insATGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381782.7:c.1524+58_1524+59insATGA MANE Select	ENSP00000371201.2:n.1524+58_1524+59insATGA
ENST00000316607.5:c.1401-1065_1401-1064insATGA	ENSP00000319127.5:n.1401-1065_1401-1064insATGA
ENST00000381782.6:c.1524+58_1524+59insATGA	ENSP00000371201.2:n.1524+58_1524+59insATGA
ENST00000423784.5:n.529+58_529+59insATGA
ENST00000478857.1:n.155+58_155+59insATGA
NM_024677.4:c.1524+58_1524+59insATGA	NP_078953.3:n.1524+58_1524+59insATGA
NM_001330648.2:c.1401-1065_1401-1064insATGA	NP_001317577.1:n.1401-1065_1401-1064insATGA
NM_024677.5:c.1524+58_1524+59insATGA	NP_078953.3:n.1524+58_1524+59insATGA
XM_017008611.2:c.1380+58_1380+59insATGA	XP_016864100.1:n.1380+58_1380+59insATGA
XM_017008612.2:c.1278+58_1278+59insATGA	XP_016864101.1:n.1278+58_1278+59insATGA
NM_024677.6:c.1524+58_1524+59insATGA MANE Select	NP_078953.4:n.1524+58_1524+59insATGA
NM_001330648.3:c.1401-1065_1401-1064insATGA	NP_001317577.1:n.1401-1065_1401-1064insATGA