Canonical Allele Identifier: CA1003041200
Gene: NEGR1 HGNC NCBI
NEGR1-IT1 HGNC NCBI

Linked Data

dbSNP Id: rs1657870101
gnomAD v3: 1-71808700-T-A
gnomAD v4: 1-71808700-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.71808700T>A , CM000663.2:g.71808700T>A GRCh38
NC_000001.10:g.72274383T>A , CM000663.1:g.72274383T>A GRCh37
NC_000001.9:g.72046971T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357731.10:c.410-32403A>T (NEGR1) MANE Select ENSP00000350364.4:n.410-32403A>T
ENST00000306821.3:c.26-32403A>T (NEGR1) ENSP00000305938.3:n.26-32403A>T
ENST00000357731.9:c.410-32403A>T (NEGR1) ENSP00000350364.4:n.410-32403A>T
ENST00000434200.5:c.245-32403A>T (NEGR1) ENSP00000413294.2:n.245-32403A>T
ENST00000467479.1:n.407-32403A>T (NEGR1)
NM_173808.2:c.410-32403A>T (NEGR1) NP_776169.2:n.410-32403A>T
NR_046218.1:n.34-10430A>T (NEGR1-IT1)
XM_011541200.1:c.410-32403A>T (NEGR1) XP_011539502.1:n.410-32403A>T
XM_011541201.1:c.410-32403A>T (NEGR1) XP_011539503.1:n.410-32403A>T
XM_011541200.3:c.410-32403A>T (NEGR1) XP_011539502.1:n.410-32403A>T
XM_011541201.3:c.410-32403A>T (NEGR1) XP_011539503.1:n.410-32403A>T
XM_017000961.2:c.410-32403A>T (NEGR1) XP_016856450.1:n.410-32403A>T
NM_173808.3:c.410-32403A>T (NEGR1) MANE Select NP_776169.2:n.410-32403A>T