Canonical Allele Identifier: CA360366936

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050922G>T (hg19) ; chr5:g.90755105G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755105G>T , CM000667.2:g.90755105G>T	GRCh38
NC_000005.9:g.90050922G>T , CM000667.1:g.90050922G>T	GRCh37
NC_000005.8:g.90086678G>T	NCBI36
NG_007083.1:g.201306G>T
NG_007083.2:g.230762G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11500G>T MANE Select	ENSP00000384582.2:p.Glu3834Ter
ENST00000425867.3:c.631G>T	ENSP00000392618.3:p.Glu211Ter
ENST00000639431.1:c.265+78896G>T	ENSP00000491057.1:n.265+78896G>T
ENST00000640374.1:n.4644G>T
ENST00000640464.1:n.1919G>T
ENST00000405460.6:c.11500G>T	ENSP00000384582.2:p.Glu3834Ter
ENST00000509621.1:c.4197G>T
NM_032119.3:c.11500G>T	NP_115495.3:p.Glu3834Ter
NR_003149.1:n.11513G>T
XM_011543675.1:c.11497G>T	XP_011541977.1:p.Glu3833Ter
XM_011543676.1:c.11419G>T	XP_011541978.1:p.Glu3807Ter
XM_011543677.1:c.8803G>T	XP_011541979.1:p.Glu2935Ter
XM_011543678.1:c.11500G>T	XP_011541980.1:p.Glu3834Ter
NM_032119.4:c.11500G>T MANE Select	NP_115495.3:p.Glu3834Ter
XM_017009963.2:c.11521G>T	XP_016865452.1:p.Glu3841Ter
XM_017009964.2:c.11518G>T	XP_016865453.1:p.Glu3840Ter
XM_017009965.1:c.11518G>T	XP_016865454.1:p.Glu3840Ter
XM_017009966.2:c.11440G>T	XP_016865455.1:p.Glu3814Ter
XM_017009967.1:c.11425G>T	XP_016865456.1:p.Glu3809Ter
XM_017009968.2:c.11521G>T	XP_016865457.1:p.Glu3841Ter
XM_017009969.2:c.11521G>T	XP_016865458.1:p.Glu3841Ter
XM_017009970.2:c.11521G>T	XP_016865459.1:p.Glu3841Ter
XM_017009971.2:c.11521G>T	XP_016865460.1:p.Glu3841Ter
XM_017009972.1:c.4639G>T	XP_016865461.1:p.Glu1547Ter
XM_017009973.1:c.4618G>T	XP_016865462.1:p.Glu1540Ter
NR_003149.2:n.11516G>T