Canonical Allele Identifier: CA2677512568

Gene: NRSN1

Linked Data

• gnomAD v4: 6-24146039-T-TGCCCACAGCTGAACACA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24146043_24146044insACAGCTGAACACAGCCC , CM000668.2:g.24146043_24146044insACAGCTGAACACAGCCC	GRCh38
NC_000006.11:g.24146271_24146272insACAGCTGAACACAGCCC , CM000668.1:g.24146271_24146272insACAGCTGAACACAGCCC	GRCh37
NC_000006.10:g.24254250_24254251insACAGCTGAACACAGCCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.*97_*98insACAGCTGAACACAGCCC MANE Select	ENSP00000367752.4:n.*97_*98insACAGCTGAACACAGCCC
ENST00000378478.5:c.*97_*98insACAGCTGAACACAGCCC	ENSP00000367739.2:n.*97_*98insACAGCTGAACACAGCCC
ENST00000378491.8:c.*97_*98insACAGCTGAACACAGCCC	ENSP00000367752.4:n.*97_*98insACAGCTGAACACAGCCC
ENST00000468195.2:n.257-8728_257-8727insACAGCTGAACACAGCCC
NM_080723.4:c.*97_*98insACAGCTGAACACAGCCC	NP_542454.3:n.*97_*98insACAGCTGAACACAGCCC
NM_080723.5:c.*97_*98insACAGCTGAACACAGCCC MANE Select	NP_542454.3:n.*97_*98insACAGCTGAACACAGCCC