Canonical Allele Identifier: CA448963157
Gene: NRSN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24145970G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145742G>T , CM000668.2:g.24145742G>T GRCh38
NC_000006.11:g.24145970G>T , CM000668.1:g.24145970G>T GRCh37
NC_000006.10:g.24253949G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.384G>T MANE Select ENSP00000367752.4:p.Thr128=
ENST00000378477.2:c.384G>T ENSP00000367738.2:p.Thr128=
ENST00000378478.5:c.384G>T ENSP00000367739.2:p.Thr128=
ENST00000378491.8:c.384G>T ENSP00000367752.4:p.Thr128=
ENST00000468195.2:n.257-9029G>T
NM_080723.4:c.384G>T NP_542454.3:p.Thr128=
NM_080723.5:c.384G>T MANE Select NP_542454.3:p.Thr128=