Canonical Allele Identifier: CA360414231

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89979887G>C (hg19) ; chr5:g.90684070G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684070G>C , CM000667.2:g.90684070G>C	GRCh38
NC_000005.9:g.89979887G>C , CM000667.1:g.89979887G>C	GRCh37
NC_000005.8:g.90015643G>C	NCBI36
NG_007083.1:g.130271G>C
NG_007083.2:g.159727G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6149G>C MANE Select	ENSP00000384582.2:p.Gly2050Ala
ENST00000639431.1:c.265+7861G>C	ENSP00000491057.1:n.265+7861G>C
ENST00000639473.1:n.1608G>C
ENST00000640012.1:c.165-1710G>C
ENST00000640403.1:c.3440G>C	ENSP00000492531.1:p.Gly1147Ala
ENST00000640779.1:c.961G>C
ENST00000405460.6:c.6149G>C	ENSP00000384582.2:p.Gly2050Ala
NM_032119.3:c.6149G>C	NP_115495.3:p.Gly2050Ala
NR_003149.1:n.6245G>C
XM_011543675.1:c.6146G>C	XP_011541977.1:p.Gly2049Ala
XM_011543676.1:c.6068G>C	XP_011541978.1:p.Gly2023Ala
XM_011543677.1:c.3452G>C	XP_011541979.1:p.Gly1151Ala
XM_011543678.1:c.6149G>C	XP_011541980.1:p.Gly2050Ala
XM_011543679.1:c.6149G>C	XP_011541981.1:p.Gly2050Ala
NM_032119.4:c.6149G>C MANE Select	NP_115495.3:p.Gly2050Ala
XM_017009963.2:c.6149G>C	XP_016865452.1:p.Gly2050Ala
XM_017009964.2:c.6146G>C	XP_016865453.1:p.Gly2049Ala
XM_017009965.1:c.6146G>C	XP_016865454.1:p.Gly2049Ala
XM_017009966.2:c.6068G>C	XP_016865455.1:p.Gly2023Ala
XM_017009967.1:c.6053G>C	XP_016865456.1:p.Gly2018Ala
XM_017009968.2:c.6149G>C	XP_016865457.1:p.Gly2050Ala
XM_017009969.2:c.6149G>C	XP_016865458.1:p.Gly2050Ala
XM_017009970.2:c.6149G>C	XP_016865459.1:p.Gly2050Ala
XM_017009971.2:c.6149G>C	XP_016865460.1:p.Gly2050Ala
XM_017009973.1:c.-651G>C	XP_016865462.1:n.-651G>C
XM_017009974.2:c.6149G>C	XP_016865463.1:p.Gly2050Ala
NR_003149.2:n.6248G>C