Canonical Allele Identifier: CA163360114

Gene: VGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.101163799G>A , CM000669.2:g.101163799G>A	GRCh38
NC_000007.13:g.100807080G>A , CM000669.1:g.100807080G>A	GRCh37
NC_000007.12:g.100593800G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249330.3:c.1045C>T MANE Select	ENSP00000249330.2:p.Arg349Trp
ENST00000249330.2:c.1045C>T	ENSP00000249330.2:p.Arg349Trp
ENST00000445482.2:c.1045C>T	ENSP00000400884.2:p.Arg349Trp
ENST00000611537.1:c.1031+12C>T	ENSP00000480817.1:n.1031+12C>T
NM_003378.3:c.1045C>T	NP_003369.2:p.Arg349Trp
XM_005250561.3:c.1045C>T	XP_005250618.1:p.Arg349Trp
XM_011516548.1:c.1045C>T	XP_011514850.1:p.Arg349Trp
XM_011516549.1:c.1045C>T	XP_011514851.1:p.Arg349Trp
XM_005250561.5:c.1045C>T	XP_005250618.1:p.Arg349Trp
XM_011516549.3:c.1045C>T	XP_011514851.1:p.Arg349Trp
NM_003378.4:c.1045C>T MANE Select	NP_003369.2:p.Arg349Trp