Canonical Allele Identifier: CA1774418348

Gene: NRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31787230_31787231delinsAT , CM000670.2:g.31787230_31787231delinsAT	GRCh38
NC_000008.10:g.31644746_31644747delinsAT , CM000670.1:g.31644746_31644747delinsAT	GRCh37
NC_000008.9:g.31764288_31764289delinsAT	NCBI36
NG_012005.1:g.152479_152480delinsAT
NG_012005.2:g.153009_153010delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519301.6:c.37+147799_37+147800delinsAT	ENSP00000429582.1:n.37+147799_37+147800delinsAT
ENST00000650856.1:c.37+147799_37+147800delinsAT	ENSP00000498216.1:n.37+147799_37+147800delinsAT
ENST00000650866.1:c.37+147799_37+147800delinsAT	ENSP00000499045.1:n.37+147799_37+147800delinsAT
ENST00000651149.1:c.37+147799_37+147800delinsAT	ENSP00000498375.1:n.37+147799_37+147800delinsAT
ENST00000651335.1:c.71+146501_71+146502delinsAT
ENST00000652698.1:c.37+147799_37+147800delinsAT	ENSP00000499008.1:n.37+147799_37+147800delinsAT
ENST00000518104.5:c.37+147799_37+147800delinsAT	ENSP00000430053.1:n.37+147799_37+147800delinsAT
ENST00000519301.5:c.37+147799_37+147800delinsAT	ENSP00000429582.1:n.37+147799_37+147800delinsAT
ENST00000520407.5:c.745+146501_745+146502delinsAT	ENSP00000434640.1:n.745+146501_745+146502delinsAT
ENST00000523534.5:c.304+146501_304+146502delinsAT	ENSP00000429067.1:n.304+146501_304+146502delinsAT
NM_001159995.1:c.37+147799_37+147800delinsAT	NP_001153467.1:n.37+147799_37+147800delinsAT
NM_001159999.1:c.37+147799_37+147800delinsAT	NP_001153471.1:n.37+147799_37+147800delinsAT
NM_001160001.1:c.37+147799_37+147800delinsAT	NP_001153473.1:n.37+147799_37+147800delinsAT
NM_013962.2:c.745+146501_745+146502delinsAT	NP_039256.2:n.745+146501_745+146502delinsAT
XM_011544512.1:c.121+146501_121+146502delinsAT	XP_011542814.1:n.121+146501_121+146502delinsAT
NM_001159995.2:c.37+147799_37+147800delinsAT	NP_001153467.1:n.37+147799_37+147800delinsAT
NM_001159999.2:c.37+147799_37+147800delinsAT	NP_001153471.1:n.37+147799_37+147800delinsAT
NM_001160001.2:c.37+147799_37+147800delinsAT	NP_001153473.1:n.37+147799_37+147800delinsAT
NM_001322201.1:c.-556+147799_-556+147800delinsAT	NP_001309130.1:n.-556+147799_-556+147800delinsAT
NM_001322202.1:c.-505+147799_-505+147800delinsAT	NP_001309131.1:n.-505+147799_-505+147800delinsAT
XM_011544512.2:c.121+146501_121+146502delinsAT	XP_011542814.1:n.121+146501_121+146502delinsAT
XM_017013365.2:c.121+146501_121+146502delinsAT	XP_016868854.1:n.121+146501_121+146502delinsAT
XM_017013366.2:c.121+146501_121+146502delinsAT	XP_016868855.1:n.121+146501_121+146502delinsAT
XM_017013367.1:c.121+146501_121+146502delinsAT	XP_016868856.1:n.121+146501_121+146502delinsAT
XM_017013371.2:c.121+146501_121+146502delinsAT	XP_016868860.1:n.121+146501_121+146502delinsAT
XM_017013372.2:c.121+146501_121+146502delinsAT	XP_016868861.1:n.121+146501_121+146502delinsAT
NM_001159995.3:c.37+147799_37+147800delinsAT	NP_001153467.1:n.37+147799_37+147800delinsAT
NM_001159999.3:c.37+147799_37+147800delinsAT	NP_001153471.1:n.37+147799_37+147800delinsAT
NM_001160001.3:c.37+147799_37+147800delinsAT	NP_001153473.1:n.37+147799_37+147800delinsAT
NM_001322201.2:c.-556+147799_-556+147800delinsAT	NP_001309130.1:n.-556+147799_-556+147800delinsAT
NM_001322202.2:c.-505+147799_-505+147800delinsAT	NP_001309131.1:n.-505+147799_-505+147800delinsAT
NM_013962.3:c.745+146501_745+146502delinsAT	NP_039256.2:n.745+146501_745+146502delinsAT