Canonical Allele Identifier: CA1174933368

Gene: NEGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.71655902C>G , CM000663.2:g.71655902C>G	GRCh38
NC_000001.10:g.72121585C>G , CM000663.1:g.72121585C>G	GRCh37
NC_000001.9:g.71894173C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_173808.3:c.667+42106G>C MANE Select	NP_776169.2:n.667+42106G>C
ENST00000357731.10:c.667+42106G>C MANE Select	ENSP00000350364.4:n.667+42106G>C
NM_173808.2:c.667+42106G>C	NP_776169.2:n.667+42106G>C
ENST00000306821.3:c.283+42106G>C	ENSP00000305938.3:n.283+42106G>C
ENST00000357731.9:c.667+42106G>C	ENSP00000350364.4:n.667+42106G>C
ENST00000434200.5:c.502+42106G>C	ENSP00000413294.2:n.502+42106G>C
XM_011541200.1:c.667+42106G>C	XP_011539502.1:n.667+42106G>C
XM_011541200.3:c.667+42106G>C	XP_011539502.1:n.667+42106G>C