Canonical Allele Identifier: CA360408923

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041446C>T (hg19) ; chr5:g.90745629C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745629C>T , CM000667.2:g.90745629C>T	GRCh38
NC_000005.9:g.90041446C>T , CM000667.1:g.90041446C>T	GRCh37
NC_000005.8:g.90077202C>T	NCBI36
NG_007083.1:g.191830C>T
NG_007083.2:g.221286C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10808C>T MANE Select	ENSP00000384582.2:p.Ala3603Val
ENST00000639431.1:c.265+69420C>T	ENSP00000491057.1:n.265+69420C>T
ENST00000640374.1:n.3952C>T
ENST00000640464.1:n.1227C>T
ENST00000405460.6:c.10808C>T	ENSP00000384582.2:p.Ala3603Val
ENST00000509621.1:c.3505C>T
NM_032119.3:c.10808C>T	NP_115495.3:p.Ala3603Val
NR_003149.1:n.10821C>T
XM_011543675.1:c.10805C>T	XP_011541977.1:p.Ala3602Val
XM_011543676.1:c.10727C>T	XP_011541978.1:p.Ala3576Val
XM_011543677.1:c.8111C>T	XP_011541979.1:p.Ala2704Val
XM_011543678.1:c.10808C>T	XP_011541980.1:p.Ala3603Val
XM_011543679.1:c.*30C>T	XP_011541981.1:n.*30C>T
NM_032119.4:c.10808C>T MANE Select	NP_115495.3:p.Ala3603Val
XM_017009963.2:c.10829C>T	XP_016865452.1:p.Ala3610Val
XM_017009964.2:c.10826C>T	XP_016865453.1:p.Ala3609Val
XM_017009965.1:c.10826C>T	XP_016865454.1:p.Ala3609Val
XM_017009966.2:c.10748C>T	XP_016865455.1:p.Ala3583Val
XM_017009967.1:c.10733C>T	XP_016865456.1:p.Ala3578Val
XM_017009968.2:c.10829C>T	XP_016865457.1:p.Ala3610Val
XM_017009969.2:c.10829C>T	XP_016865458.1:p.Ala3610Val
XM_017009970.2:c.10829C>T	XP_016865459.1:p.Ala3610Val
XM_017009971.2:c.10829C>T	XP_016865460.1:p.Ala3610Val
XM_017009972.1:c.3947C>T	XP_016865461.1:p.Ala1316Val
XM_017009973.1:c.3926C>T	XP_016865462.1:p.Ala1309Val
XM_017009974.2:c.*30C>T	XP_016865463.1:n.*30C>T
NR_003149.2:n.10824C>T