Canonical Allele Identifier: CA360414243

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89979893A>G (hg19) ; chr5:g.90684076A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684076A>G , CM000667.2:g.90684076A>G	GRCh38
NC_000005.9:g.89979893A>G , CM000667.1:g.89979893A>G	GRCh37
NC_000005.8:g.90015649A>G	NCBI36
NG_007083.1:g.130277A>G
NG_007083.2:g.159733A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6155A>G MANE Select	ENSP00000384582.2:p.Asn2052Ser
ENST00000639431.1:c.265+7867A>G	ENSP00000491057.1:n.265+7867A>G
ENST00000639473.1:n.1614A>G
ENST00000640012.1:c.165-1704A>G
ENST00000640403.1:c.3446A>G	ENSP00000492531.1:p.Asn1149Ser
ENST00000640779.1:c.967A>G
ENST00000405460.6:c.6155A>G	ENSP00000384582.2:p.Asn2052Ser
NM_032119.3:c.6155A>G	NP_115495.3:p.Asn2052Ser
NR_003149.1:n.6251A>G
XM_011543675.1:c.6152A>G	XP_011541977.1:p.Asn2051Ser
XM_011543676.1:c.6074A>G	XP_011541978.1:p.Asn2025Ser
XM_011543677.1:c.3458A>G	XP_011541979.1:p.Asn1153Ser
XM_011543678.1:c.6155A>G	XP_011541980.1:p.Asn2052Ser
XM_011543679.1:c.6155A>G	XP_011541981.1:p.Asn2052Ser
NM_032119.4:c.6155A>G MANE Select	NP_115495.3:p.Asn2052Ser
XM_017009963.2:c.6155A>G	XP_016865452.1:p.Asn2052Ser
XM_017009964.2:c.6152A>G	XP_016865453.1:p.Asn2051Ser
XM_017009965.1:c.6152A>G	XP_016865454.1:p.Asn2051Ser
XM_017009966.2:c.6074A>G	XP_016865455.1:p.Asn2025Ser
XM_017009967.1:c.6059A>G	XP_016865456.1:p.Asn2020Ser
XM_017009968.2:c.6155A>G	XP_016865457.1:p.Asn2052Ser
XM_017009969.2:c.6155A>G	XP_016865458.1:p.Asn2052Ser
XM_017009970.2:c.6155A>G	XP_016865459.1:p.Asn2052Ser
XM_017009971.2:c.6155A>G	XP_016865460.1:p.Asn2052Ser
XM_017009973.1:c.-645A>G	XP_016865462.1:n.-645A>G
XM_017009974.2:c.6155A>G	XP_016865463.1:p.Asn2052Ser
NR_003149.2:n.6254A>G