Canonical Allele Identifier: CA445406338

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059133T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763316T>C , CM000667.2:g.90763316T>C	GRCh38
NC_000005.9:g.90059133T>C , CM000667.1:g.90059133T>C	GRCh37
NC_000005.8:g.90094889T>C	NCBI36
NG_007083.1:g.209517T>C
NG_007083.2:g.238973T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12132T>C MANE Select	ENSP00000384582.2:p.Asp4044=
ENST00000425867.3:c.1086T>C	ENSP00000392618.3:p.Asp362=
ENST00000639431.1:c.265+87107T>C	ENSP00000491057.1:n.265+87107T>C
ENST00000640464.1:n.2551T>C
ENST00000640729.1:n.709T>C
ENST00000405460.6:c.12132T>C	ENSP00000384582.2:p.Asp4044=
NM_032119.3:c.12132T>C	NP_115495.3:p.Asp4044=
NR_003149.1:n.12145T>C
XM_011543675.1:c.12129T>C	XP_011541977.1:p.Asp4043=
XM_011543676.1:c.12051T>C	XP_011541978.1:p.Asp4017=
XM_011543677.1:c.9435T>C	XP_011541979.1:p.Asp3145=
XM_011543678.1:c.12132T>C	XP_011541980.1:p.Asp4044=
NM_032119.4:c.12132T>C MANE Select	NP_115495.3:p.Asp4044=
XM_017009963.2:c.12153T>C	XP_016865452.1:p.Asp4051=
XM_017009964.2:c.12150T>C	XP_016865453.1:p.Asp4050=
XM_017009965.1:c.12150T>C	XP_016865454.1:p.Asp4050=
XM_017009966.2:c.12072T>C	XP_016865455.1:p.Asp4024=
XM_017009967.1:c.12057T>C	XP_016865456.1:p.Asp4019=
XM_017009968.2:c.12153T>C	XP_016865457.1:p.Asp4051=
XM_017009969.2:c.12153T>C	XP_016865458.1:p.Asp4051=
XM_017009970.2:c.12153T>C	XP_016865459.1:p.Asp4051=
XM_017009971.2:c.12153T>C	XP_016865460.1:p.Asp4051=
XM_017009972.1:c.5271T>C	XP_016865461.1:p.Asp1757=
XM_017009973.1:c.5250T>C	XP_016865462.1:p.Asp1750=
NR_003149.2:n.12148T>C