Canonical Allele Identifier: CA445404582

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988574T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692757T>C , CM000667.2:g.90692757T>C	GRCh38
NC_000005.9:g.89988574T>C , CM000667.1:g.89988574T>C	GRCh37
NC_000005.8:g.90024330T>C	NCBI36
NG_007083.1:g.138958T>C
NG_007083.2:g.168414T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7104T>C MANE Select	ENSP00000384582.2:p.Ser2368=
ENST00000639431.1:c.265+16548T>C	ENSP00000491057.1:n.265+16548T>C
ENST00000639473.1:n.2563T>C
ENST00000640012.1:c.911T>C
ENST00000640374.1:n.248T>C
ENST00000640403.1:c.4395T>C	ENSP00000492531.1:p.Ser1465=
ENST00000640779.1:c.1833T>C
ENST00000405460.6:c.7104T>C	ENSP00000384582.2:p.Ser2368=
NM_032119.3:c.7104T>C	NP_115495.3:p.Ser2368=
NR_003149.1:n.7117T>C
XM_011543675.1:c.7101T>C	XP_011541977.1:p.Ser2367=
XM_011543676.1:c.7023T>C	XP_011541978.1:p.Ser2341=
XM_011543677.1:c.4407T>C	XP_011541979.1:p.Ser1469=
XM_011543678.1:c.7104T>C	XP_011541980.1:p.Ser2368=
XM_011543679.1:c.7104T>C	XP_011541981.1:p.Ser2368=
NM_032119.4:c.7104T>C MANE Select	NP_115495.3:p.Ser2368=
XM_017009963.2:c.7104T>C	XP_016865452.1:p.Ser2368=
XM_017009964.2:c.7101T>C	XP_016865453.1:p.Ser2367=
XM_017009965.1:c.7101T>C	XP_016865454.1:p.Ser2367=
XM_017009966.2:c.7023T>C	XP_016865455.1:p.Ser2341=
XM_017009967.1:c.7008T>C	XP_016865456.1:p.Ser2336=
XM_017009968.2:c.7104T>C	XP_016865457.1:p.Ser2368=
XM_017009969.2:c.7104T>C	XP_016865458.1:p.Ser2368=
XM_017009970.2:c.7104T>C	XP_016865459.1:p.Ser2368=
XM_017009971.2:c.7104T>C	XP_016865460.1:p.Ser2368=
XM_017009972.1:c.222T>C	XP_016865461.1:p.Ser74=
XM_017009973.1:c.222T>C	XP_016865462.1:p.Ser74=
XM_017009974.2:c.7104T>C	XP_016865463.1:p.Ser2368=
NR_003149.2:n.7120T>C