Canonical Allele Identifier: CA12892156
Gene: NRG1 HGNC NCBI
NRG1-IT1 HGNC NCBI

Linked Data

dbSNP Id: rs1462906
gnomAD v2: 8-31896592-T-C
gnomAD v3: 8-32039076-T-C
gnomAD v4: 8-32039076-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.32039076T>C , CM000670.2:g.32039076T>C GRCh38
NC_000008.10:g.31896592T>C , CM000670.1:g.31896592T>C GRCh37
NC_000008.9:g.32016134T>C NCBI36
NG_012005.1:g.404325T>C
NG_012005.2:g.404855T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000519301.6:c.37+399645T>C (NRG1) ENSP00000429582.1:n.37+399645T>C
ENST00000650856.1:c.37+399645T>C (NRG1) ENSP00000498216.1:n.37+399645T>C
ENST00000650866.1:c.37+399645T>C (NRG1) ENSP00000499045.1:n.37+399645T>C
ENST00000651149.1:c.37+399645T>C (NRG1) ENSP00000498375.1:n.37+399645T>C
ENST00000651335.1:c.71+398347T>C (NRG1)
ENST00000652698.1:c.37+399645T>C (NRG1) ENSP00000499008.1:n.37+399645T>C
ENST00000518104.5:c.37+399645T>C (NRG1) ENSP00000430053.1:n.37+399645T>C
ENST00000519301.5:c.37+399645T>C (NRG1) ENSP00000429582.1:n.37+399645T>C
ENST00000520407.5:c.745+398347T>C (NRG1) ENSP00000434640.1:n.745+398347T>C
ENST00000523534.5:c.304+398347T>C (NRG1) ENSP00000429067.1:n.304+398347T>C
NM_001159995.1:c.37+399645T>C (NRG1) NP_001153467.1:n.37+399645T>C
NM_001159999.1:c.37+399645T>C (NRG1) NP_001153471.1:n.37+399645T>C
NM_001160001.1:c.37+399645T>C (NRG1) NP_001153473.1:n.37+399645T>C
NM_013962.2:c.745+398347T>C (NRG1) NP_039256.2:n.745+398347T>C
NR_104156.1:n.338+8617T>C (NRG1-IT1)
NR_104157.1:n.254+9591T>C (NRG1-IT1)
NR_104158.1:n.136+9591T>C (NRG1-IT1)
XM_011544512.1:c.121+398347T>C (NRG1) XP_011542814.1:n.121+398347T>C
NM_001159995.2:c.37+399645T>C (NRG1) NP_001153467.1:n.37+399645T>C
NM_001159999.2:c.37+399645T>C (NRG1) NP_001153471.1:n.37+399645T>C
NM_001160001.2:c.37+399645T>C (NRG1) NP_001153473.1:n.37+399645T>C
NM_001322201.1:c.-556+399645T>C (NRG1) NP_001309130.1:n.-556+399645T>C
NM_001322202.1:c.-505+399645T>C (NRG1) NP_001309131.1:n.-505+399645T>C
XM_011544512.2:c.121+398347T>C (NRG1) XP_011542814.1:n.121+398347T>C
XM_017013365.2:c.121+398347T>C (NRG1) XP_016868854.1:n.121+398347T>C
XM_017013366.2:c.121+398347T>C (NRG1) XP_016868855.1:n.121+398347T>C
XM_017013367.1:c.121+398347T>C (NRG1) XP_016868856.1:n.121+398347T>C
XM_017013371.2:c.121+398347T>C (NRG1) XP_016868860.1:n.121+398347T>C
XM_017013372.2:c.121+398347T>C (NRG1) XP_016868861.1:n.121+398347T>C
NM_001159995.3:c.37+399645T>C (NRG1) NP_001153467.1:n.37+399645T>C
NM_001159999.3:c.37+399645T>C (NRG1) NP_001153471.1:n.37+399645T>C
NM_001160001.3:c.37+399645T>C (NRG1) NP_001153473.1:n.37+399645T>C
NM_001322201.2:c.-556+399645T>C (NRG1) NP_001309130.1:n.-556+399645T>C
NM_001322202.2:c.-505+399645T>C (NRG1) NP_001309131.1:n.-505+399645T>C
NM_013962.3:c.745+398347T>C (NRG1) NP_039256.2:n.745+398347T>C