Canonical Allele Identifier: CA1774597653

Gene: NRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.32169015_32169016delinsTG , CM000670.2:g.32169015_32169016delinsTG	GRCh38
NC_000008.10:g.32026531_32026532delinsTG , CM000670.1:g.32026531_32026532delinsTG	GRCh37
NC_000008.9:g.32146073_32146074delinsTG	NCBI36
NG_012005.1:g.534264_534265delinsTG
NG_012005.2:g.534794_534795delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519301.6:c.38-426813_38-426812delinsTG	ENSP00000429582.1:n.38-426813_38-426812delinsTG
ENST00000650856.1:c.38-426813_38-426812delinsTG	ENSP00000498216.1:n.38-426813_38-426812delinsTG
ENST00000650866.1:c.38-426813_38-426812delinsTG	ENSP00000499045.1:n.38-426813_38-426812delinsTG
ENST00000651149.1:c.38-426813_38-426812delinsTG	ENSP00000498375.1:n.38-426813_38-426812delinsTG
ENST00000651335.1:c.72-426813_72-426812delinsTG
ENST00000652698.1:c.38-426813_38-426812delinsTG	ENSP00000499008.1:n.38-426813_38-426812delinsTG
ENST00000518104.5:c.38-426813_38-426812delinsTG	ENSP00000430053.1:n.38-426813_38-426812delinsTG
ENST00000519301.5:c.38-426813_38-426812delinsTG	ENSP00000429582.1:n.38-426813_38-426812delinsTG
ENST00000520407.5:c.746-426813_746-426812delinsTG	ENSP00000434640.1:n.746-426813_746-426812delinsTG
ENST00000523534.5:c.305-426813_305-426812delinsTG	ENSP00000429067.1:n.305-426813_305-426812delinsTG
NM_001159995.1:c.38-426813_38-426812delinsTG	NP_001153467.1:n.38-426813_38-426812delinsTG
NM_001159999.1:c.38-426813_38-426812delinsTG	NP_001153471.1:n.38-426813_38-426812delinsTG
NM_001160001.1:c.38-426813_38-426812delinsTG	NP_001153473.1:n.38-426813_38-426812delinsTG
NM_013962.2:c.746-426813_746-426812delinsTG	NP_039256.2:n.746-426813_746-426812delinsTG
XM_011544512.1:c.122-426813_122-426812delinsTG	XP_011542814.1:n.122-426813_122-426812delinsTG
NM_001159995.2:c.38-426813_38-426812delinsTG	NP_001153467.1:n.38-426813_38-426812delinsTG
NM_001159999.2:c.38-426813_38-426812delinsTG	NP_001153471.1:n.38-426813_38-426812delinsTG
NM_001160001.2:c.38-426813_38-426812delinsTG	NP_001153473.1:n.38-426813_38-426812delinsTG
NM_001322201.1:c.-555-426813_-555-426812delinsTG	NP_001309130.1:n.-555-426813_-555-426812delinsTG
NM_001322202.1:c.-504-426813_-504-426812delinsTG	NP_001309131.1:n.-504-426813_-504-426812delinsTG
XM_011544512.2:c.122-426813_122-426812delinsTG	XP_011542814.1:n.122-426813_122-426812delinsTG
XM_017013365.2:c.122-426813_122-426812delinsTG	XP_016868854.1:n.122-426813_122-426812delinsTG
XM_017013366.2:c.122-426813_122-426812delinsTG	XP_016868855.1:n.122-426813_122-426812delinsTG
XM_017013367.1:c.122-426813_122-426812delinsTG	XP_016868856.1:n.122-426813_122-426812delinsTG
XM_017013371.2:c.122-426813_122-426812delinsTG	XP_016868860.1:n.122-426813_122-426812delinsTG
XM_017013372.2:c.122-426813_122-426812delinsTG	XP_016868861.1:n.122-426813_122-426812delinsTG
NM_001159995.3:c.38-426813_38-426812delinsTG	NP_001153467.1:n.38-426813_38-426812delinsTG
NM_001159999.3:c.38-426813_38-426812delinsTG	NP_001153471.1:n.38-426813_38-426812delinsTG
NM_001160001.3:c.38-426813_38-426812delinsTG	NP_001153473.1:n.38-426813_38-426812delinsTG
NM_001322201.2:c.-555-426813_-555-426812delinsTG	NP_001309130.1:n.-555-426813_-555-426812delinsTG
NM_001322202.2:c.-504-426813_-504-426812delinsTG	NP_001309131.1:n.-504-426813_-504-426812delinsTG
NM_013962.3:c.746-426813_746-426812delinsTG	NP_039256.2:n.746-426813_746-426812delinsTG