Canonical Allele Identifier: CA4406352

Gene: VGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.101164100C>G , CM000669.2:g.101164100C>G	GRCh38
NC_000007.13:g.100807381C>G , CM000669.1:g.100807381C>G	GRCh37
NC_000007.12:g.100594101C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249330.3:c.744G>C MANE Select	ENSP00000249330.2:p.Gly248=
ENST00000249330.2:c.744G>C	ENSP00000249330.2:p.Gly248=
ENST00000445482.2:c.744G>C	ENSP00000400884.2:p.Gly248=
ENST00000611537.1:c.744G>C	ENSP00000480817.1:p.Gly248=
NM_003378.3:c.744G>C	NP_003369.2:p.Gly248=
XM_005250561.3:c.744G>C	XP_005250618.1:p.Gly248=
XM_011516548.1:c.744G>C	XP_011514850.1:p.Gly248=
XM_011516549.1:c.744G>C	XP_011514851.1:p.Gly248=
XM_005250561.5:c.744G>C	XP_005250618.1:p.Gly248=
XM_011516549.3:c.744G>C	XP_011514851.1:p.Gly248=
NM_003378.4:c.744G>C MANE Select	NP_003369.2:p.Gly248=