Canonical Allele Identifier: CA1774794606

Gene: NRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.32595844G= , CM000670.2:g.32595844G=	GRCh38
NC_000008.10:g.32453362G= , CM000670.1:g.32453362G=	GRCh37
NC_000008.9:g.32572904G=	NCBI36
NG_012005.1:g.961095G=
NG_012005.2:g.961623G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405005.8:c.117G= MANE Select	ENSP00000384620.2:p.Leu39=
ENST00000519301.6:c.54G=	ENSP00000429582.1:p.Leu18=
ENST00000650856.1:c.54G=	ENSP00000498216.1:p.Leu18=
ENST00000650866.1:c.54G=	ENSP00000499045.1:p.Leu18=
ENST00000650919.1:c.117G=	ENSP00000498811.1:p.Leu39=
ENST00000650964.1:n.114G=
ENST00000650967.1:c.117G=	ENSP00000498833.1:p.Leu39=
ENST00000650980.1:c.117G=	ENSP00000498583.1:p.Leu39=
ENST00000651149.1:c.54G=	ENSP00000498375.1:p.Leu18=
ENST00000651175.1:n.114G=
ENST00000651335.1:c.88G=
ENST00000651807.1:n.554G=
ENST00000652588.1:c.231G=	ENSP00000498367.1:p.Leu77=
ENST00000652698.1:c.54G=	ENSP00000499008.1:p.Leu18=
ENST00000287842.7:c.117G=	ENSP00000287842.4:p.Leu39=
ENST00000356819.7:c.117G=	ENSP00000349275.6:p.Leu39=
ENST00000405005.7:c.117G=	ENSP00000384620.2:p.Leu39=
ENST00000518104.5:c.54G=	ENSP00000430053.1:p.Leu18=
ENST00000519301.5:c.54G=	ENSP00000429582.1:p.Leu18=
ENST00000520407.5:c.762G=	ENSP00000434640.1:p.Leu254=
ENST00000521670.5:c.117G=	ENSP00000428828.1:p.Leu39=
ENST00000523079.5:c.117G=	ENSP00000430120.1:p.Leu39=
ENST00000523534.5:c.321G=	ENSP00000429067.1:p.Leu107=
ENST00000631040.2:c.66G=	ENSP00000486375.1:p.Leu22=
NM_001159995.1:c.54G=	NP_001153467.1:p.Leu18=
NM_001159999.1:c.54G=	NP_001153471.1:p.Leu18=
NM_001160001.1:c.54G=	NP_001153473.1:p.Leu18=
NM_001160002.1:c.117G=	NP_001153474.1:p.Leu39=
NM_001160004.1:c.117G=	NP_001153476.1:p.Leu39=
NM_001160005.1:c.117G=	NP_001153477.1:p.Leu39=
NM_001160007.1:c.117G=	NP_001153479.1:p.Leu39=
NM_001160008.1:c.117G=	NP_001153480.1:p.Leu39=
NM_004495.3:c.117G=	NP_004486.2:p.Leu39=
NM_013956.3:c.117G=	NP_039250.2:p.Leu39=
NM_013957.3:c.117G=	NP_039251.2:p.Leu39=
NM_013958.3:c.117G=	NP_039252.2:p.Leu39=
NM_013960.3:c.117G=	NP_039254.1:p.Leu39=
NM_013962.2:c.762G=	NP_039256.2:p.Leu254=
NM_013964.3:c.117G=	NP_039258.1:p.Leu39=
XM_011544512.1:c.138G=	XP_011542814.1:p.Leu46=
NM_001159995.2:c.54G=	NP_001153467.1:p.Leu18=
NM_001159999.2:c.54G=	NP_001153471.1:p.Leu18=
NM_001160001.2:c.54G=	NP_001153473.1:p.Leu18=
NM_001160004.2:c.117G=	NP_001153476.1:p.Leu39=
NM_001322201.1:c.-539G=	NP_001309130.1:n.-539G=
NM_001322202.1:c.-488G=	NP_001309131.1:n.-488G=
NM_013956.4:c.117G=	NP_039250.2:p.Leu39=
NM_013957.4:c.117G=	NP_039251.2:p.Leu39=
NM_013960.4:c.117G=	NP_039254.1:p.Leu39=
NM_013964.4:c.117G=	NP_039258.1:p.Leu39=
XM_011544512.2:c.138G=	XP_011542814.1:p.Leu46=
XM_017013365.2:c.138G=	XP_016868854.1:p.Leu46=
XM_017013366.2:c.138G=	XP_016868855.1:p.Leu46=
XM_017013367.1:c.138G=	XP_016868856.1:p.Leu46=
XM_017013368.2:c.117G=	XP_016868857.1:p.Leu39=
XM_017013371.2:c.138G=	XP_016868860.1:p.Leu46=
XM_017013372.2:c.138G=	XP_016868861.1:p.Leu46=
XM_024447143.1:c.117G=	XP_024302911.1:p.Leu39=
NM_001159995.3:c.54G=	NP_001153467.1:p.Leu18=
NM_001159999.3:c.54G=	NP_001153471.1:p.Leu18=
NM_001160001.3:c.54G=	NP_001153473.1:p.Leu18=
NM_001160002.2:c.117G=	NP_001153474.1:p.Leu39=
NM_001160004.3:c.117G=	NP_001153476.1:p.Leu39=
NM_001160007.2:c.117G=	NP_001153479.1:p.Leu39=
NM_001160008.2:c.117G=	NP_001153480.1:p.Leu39=
NM_001322201.2:c.-539G=	NP_001309130.1:n.-539G=
NM_001322202.2:c.-488G=	NP_001309131.1:n.-488G=
NM_004495.4:c.117G=	NP_004486.2:p.Leu39=
NM_013956.5:c.117G=	NP_039250.2:p.Leu39=
NM_013957.5:c.117G=	NP_039251.2:p.Leu39=
NM_013960.5:c.117G=	NP_039254.1:p.Leu39=
NM_013964.5:c.117G= MANE Select	NP_039258.1:p.Leu39=
NM_001160005.2:c.117G=	NP_001153477.1:p.Leu39=
NM_013958.4:c.117G=	NP_039252.2:p.Leu39=
NM_013962.3:c.762G=	NP_039256.2:p.Leu254=