Canonical Allele Identifier: CA445416020

Gene: ADGRV1

Linked Data

• COSMIC: COSM6470583
• MyVariant Identifiers: chr5:g.90041411A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745594A>T , CM000667.2:g.90745594A>T	GRCh38
NC_000005.9:g.90041411A>T , CM000667.1:g.90041411A>T	GRCh37
NC_000005.8:g.90077167A>T	NCBI36
NG_007083.1:g.191795A>T
NG_007083.2:g.221251A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10773A>T MANE Select	ENSP00000384582.2:p.Ser3591=
ENST00000639431.1:c.265+69385A>T	ENSP00000491057.1:n.265+69385A>T
ENST00000640374.1:n.3917A>T
ENST00000640464.1:n.1192A>T
ENST00000405460.6:c.10773A>T	ENSP00000384582.2:p.Ser3591=
ENST00000509621.1:c.3470A>T
NM_032119.3:c.10773A>T	NP_115495.3:p.Ser3591=
NR_003149.1:n.10786A>T
XM_011543675.1:c.10770A>T	XP_011541977.1:p.Ser3590=
XM_011543676.1:c.10692A>T	XP_011541978.1:p.Ser3564=
XM_011543677.1:c.8076A>T	XP_011541979.1:p.Ser2692=
XM_011543678.1:c.10773A>T	XP_011541980.1:p.Ser3591=
XM_011543679.1:c.10770-2A>T	XP_011541981.1:n.10770-2A>T
NM_032119.4:c.10773A>T MANE Select	NP_115495.3:p.Ser3591=
XM_017009963.2:c.10794A>T	XP_016865452.1:p.Ser3598=
XM_017009964.2:c.10791A>T	XP_016865453.1:p.Ser3597=
XM_017009965.1:c.10791A>T	XP_016865454.1:p.Ser3597=
XM_017009966.2:c.10713A>T	XP_016865455.1:p.Ser3571=
XM_017009967.1:c.10698A>T	XP_016865456.1:p.Ser3566=
XM_017009968.2:c.10794A>T	XP_016865457.1:p.Ser3598=
XM_017009969.2:c.10794A>T	XP_016865458.1:p.Ser3598=
XM_017009970.2:c.10794A>T	XP_016865459.1:p.Ser3598=
XM_017009971.2:c.10794A>T	XP_016865460.1:p.Ser3598=
XM_017009972.1:c.3912A>T	XP_016865461.1:p.Ser1304=
XM_017009973.1:c.3891A>T	XP_016865462.1:p.Ser1297=
XM_017009974.2:c.10791-2A>T	XP_016865463.1:n.10791-2A>T
NR_003149.2:n.10789A>T