Canonical Allele Identifier: CA360367294

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050977C>T (hg19) ; chr5:g.90755160C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755160C>T , CM000667.2:g.90755160C>T	GRCh38
NC_000005.9:g.90050977C>T , CM000667.1:g.90050977C>T	GRCh37
NC_000005.8:g.90086733C>T	NCBI36
NG_007083.1:g.201361C>T
NG_007083.2:g.230817C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11555C>T MANE Select	ENSP00000384582.2:p.Ala3852Val
ENST00000425867.3:c.686C>T	ENSP00000392618.3:p.Ala229Val
ENST00000639431.1:c.265+78951C>T	ENSP00000491057.1:n.265+78951C>T
ENST00000640374.1:n.4699C>T
ENST00000640464.1:n.1974C>T
ENST00000405460.6:c.11555C>T	ENSP00000384582.2:p.Ala3852Val
ENST00000509621.1:c.4252C>T
NM_032119.3:c.11555C>T	NP_115495.3:p.Ala3852Val
NR_003149.1:n.11568C>T
XM_011543675.1:c.11552C>T	XP_011541977.1:p.Ala3851Val
XM_011543676.1:c.11474C>T	XP_011541978.1:p.Ala3825Val
XM_011543677.1:c.8858C>T	XP_011541979.1:p.Ala2953Val
XM_011543678.1:c.11555C>T	XP_011541980.1:p.Ala3852Val
NM_032119.4:c.11555C>T MANE Select	NP_115495.3:p.Ala3852Val
XM_017009963.2:c.11576C>T	XP_016865452.1:p.Ala3859Val
XM_017009964.2:c.11573C>T	XP_016865453.1:p.Ala3858Val
XM_017009965.1:c.11573C>T	XP_016865454.1:p.Ala3858Val
XM_017009966.2:c.11495C>T	XP_016865455.1:p.Ala3832Val
XM_017009967.1:c.11480C>T	XP_016865456.1:p.Ala3827Val
XM_017009968.2:c.11576C>T	XP_016865457.1:p.Ala3859Val
XM_017009969.2:c.11576C>T	XP_016865458.1:p.Ala3859Val
XM_017009970.2:c.11576C>T	XP_016865459.1:p.Ala3859Val
XM_017009971.2:c.11576C>T	XP_016865460.1:p.Ala3859Val
XM_017009972.1:c.4694C>T	XP_016865461.1:p.Ala1565Val
XM_017009973.1:c.4673C>T	XP_016865462.1:p.Ala1558Val
NR_003149.2:n.11571C>T