Canonical Allele Identifier: CA360414236

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89979890C>T (hg19) ; chr5:g.90684073C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684073C>T , CM000667.2:g.90684073C>T	GRCh38
NC_000005.9:g.89979890C>T , CM000667.1:g.89979890C>T	GRCh37
NC_000005.8:g.90015646C>T	NCBI36
NG_007083.1:g.130274C>T
NG_007083.2:g.159730C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6152C>T MANE Select	ENSP00000384582.2:p.Ala2051Val
ENST00000639431.1:c.265+7864C>T	ENSP00000491057.1:n.265+7864C>T
ENST00000639473.1:n.1611C>T
ENST00000640012.1:c.165-1707C>T
ENST00000640403.1:c.3443C>T	ENSP00000492531.1:p.Ala1148Val
ENST00000640779.1:c.964C>T
ENST00000405460.6:c.6152C>T	ENSP00000384582.2:p.Ala2051Val
NM_032119.3:c.6152C>T	NP_115495.3:p.Ala2051Val
NR_003149.1:n.6248C>T
XM_011543675.1:c.6149C>T	XP_011541977.1:p.Ala2050Val
XM_011543676.1:c.6071C>T	XP_011541978.1:p.Ala2024Val
XM_011543677.1:c.3455C>T	XP_011541979.1:p.Ala1152Val
XM_011543678.1:c.6152C>T	XP_011541980.1:p.Ala2051Val
XM_011543679.1:c.6152C>T	XP_011541981.1:p.Ala2051Val
NM_032119.4:c.6152C>T MANE Select	NP_115495.3:p.Ala2051Val
XM_017009963.2:c.6152C>T	XP_016865452.1:p.Ala2051Val
XM_017009964.2:c.6149C>T	XP_016865453.1:p.Ala2050Val
XM_017009965.1:c.6149C>T	XP_016865454.1:p.Ala2050Val
XM_017009966.2:c.6071C>T	XP_016865455.1:p.Ala2024Val
XM_017009967.1:c.6056C>T	XP_016865456.1:p.Ala2019Val
XM_017009968.2:c.6152C>T	XP_016865457.1:p.Ala2051Val
XM_017009969.2:c.6152C>T	XP_016865458.1:p.Ala2051Val
XM_017009970.2:c.6152C>T	XP_016865459.1:p.Ala2051Val
XM_017009971.2:c.6152C>T	XP_016865460.1:p.Ala2051Val
XM_017009973.1:c.-648C>T	XP_016865462.1:n.-648C>T
XM_017009974.2:c.6152C>T	XP_016865463.1:p.Ala2051Val
NR_003149.2:n.6251C>T