Canonical Allele Identifier: CA850850503

Gene: NRG1

Linked Data

• dbSNP Id: rs1174483474
• MyVariant Identifiers: chr8:g.32026431_32026476del (hg19) ; chr8:g.32168915_32168960del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.32168916_32168961del , CM000670.2:g.32168916_32168961del	GRCh38
NC_000008.10:g.32026432_32026477del , CM000670.1:g.32026432_32026477del	GRCh37
NC_000008.9:g.32145974_32146019del	NCBI36
NG_012005.1:g.534165_534210del
NG_012005.2:g.534695_534740del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519301.6:c.38-426912_38-426867del	ENSP00000429582.1:n.38-426912_38-426867del
ENST00000650856.1:c.38-426912_38-426867del	ENSP00000498216.1:n.38-426912_38-426867del
ENST00000650866.1:c.38-426912_38-426867del	ENSP00000499045.1:n.38-426912_38-426867del
ENST00000651149.1:c.38-426912_38-426867del	ENSP00000498375.1:n.38-426912_38-426867del
ENST00000651335.1:c.72-426912_72-426867del
ENST00000652698.1:c.38-426912_38-426867del	ENSP00000499008.1:n.38-426912_38-426867del
ENST00000518104.5:c.38-426912_38-426867del	ENSP00000430053.1:n.38-426912_38-426867del
ENST00000519301.5:c.38-426912_38-426867del	ENSP00000429582.1:n.38-426912_38-426867del
ENST00000520407.5:c.746-426912_746-426867del	ENSP00000434640.1:n.746-426912_746-426867del
ENST00000523534.5:c.305-426912_305-426867del	ENSP00000429067.1:n.305-426912_305-426867del
NM_001159995.1:c.38-426912_38-426867del	NP_001153467.1:n.38-426912_38-426867del
NM_001159999.1:c.38-426912_38-426867del	NP_001153471.1:n.38-426912_38-426867del
NM_001160001.1:c.38-426912_38-426867del	NP_001153473.1:n.38-426912_38-426867del
NM_013962.2:c.746-426912_746-426867del	NP_039256.2:n.746-426912_746-426867del
XM_011544512.1:c.122-426912_122-426867del	XP_011542814.1:n.122-426912_122-426867del
NM_001159995.2:c.38-426912_38-426867del	NP_001153467.1:n.38-426912_38-426867del
NM_001159999.2:c.38-426912_38-426867del	NP_001153471.1:n.38-426912_38-426867del
NM_001160001.2:c.38-426912_38-426867del	NP_001153473.1:n.38-426912_38-426867del
NM_001322201.1:c.-555-426912_-555-426867del	NP_001309130.1:n.-555-426912_-555-426867del
NM_001322202.1:c.-504-426912_-504-426867del	NP_001309131.1:n.-504-426912_-504-426867del
XM_011544512.2:c.122-426912_122-426867del	XP_011542814.1:n.122-426912_122-426867del
XM_017013365.2:c.122-426912_122-426867del	XP_016868854.1:n.122-426912_122-426867del
XM_017013366.2:c.122-426912_122-426867del	XP_016868855.1:n.122-426912_122-426867del
XM_017013367.1:c.122-426912_122-426867del	XP_016868856.1:n.122-426912_122-426867del
XM_017013371.2:c.122-426912_122-426867del	XP_016868860.1:n.122-426912_122-426867del
XM_017013372.2:c.122-426912_122-426867del	XP_016868861.1:n.122-426912_122-426867del
NM_001159995.3:c.38-426912_38-426867del	NP_001153467.1:n.38-426912_38-426867del
NM_001159999.3:c.38-426912_38-426867del	NP_001153471.1:n.38-426912_38-426867del
NM_001160001.3:c.38-426912_38-426867del	NP_001153473.1:n.38-426912_38-426867del
NM_001322201.2:c.-555-426912_-555-426867del	NP_001309130.1:n.-555-426912_-555-426867del
NM_001322202.2:c.-504-426912_-504-426867del	NP_001309131.1:n.-504-426912_-504-426867del
NM_013962.3:c.746-426912_746-426867del	NP_039256.2:n.746-426912_746-426867del