Canonical Allele Identifier: CA360367029

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050935T>A (hg19) ; chr5:g.90755118T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755118T>A , CM000667.2:g.90755118T>A	GRCh38
NC_000005.9:g.90050935T>A , CM000667.1:g.90050935T>A	GRCh37
NC_000005.8:g.90086691T>A	NCBI36
NG_007083.1:g.201319T>A
NG_007083.2:g.230775T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11513T>A MANE Select	ENSP00000384582.2:p.Leu3838Ter
ENST00000425867.3:c.644T>A	ENSP00000392618.3:p.Leu215Ter
ENST00000639431.1:c.265+78909T>A	ENSP00000491057.1:n.265+78909T>A
ENST00000640374.1:n.4657T>A
ENST00000640464.1:n.1932T>A
ENST00000405460.6:c.11513T>A	ENSP00000384582.2:p.Leu3838Ter
ENST00000509621.1:c.4210T>A
NM_032119.3:c.11513T>A	NP_115495.3:p.Leu3838Ter
NR_003149.1:n.11526T>A
XM_011543675.1:c.11510T>A	XP_011541977.1:p.Leu3837Ter
XM_011543676.1:c.11432T>A	XP_011541978.1:p.Leu3811Ter
XM_011543677.1:c.8816T>A	XP_011541979.1:p.Leu2939Ter
XM_011543678.1:c.11513T>A	XP_011541980.1:p.Leu3838Ter
NM_032119.4:c.11513T>A MANE Select	NP_115495.3:p.Leu3838Ter
XM_017009963.2:c.11534T>A	XP_016865452.1:p.Leu3845Ter
XM_017009964.2:c.11531T>A	XP_016865453.1:p.Leu3844Ter
XM_017009965.1:c.11531T>A	XP_016865454.1:p.Leu3844Ter
XM_017009966.2:c.11453T>A	XP_016865455.1:p.Leu3818Ter
XM_017009967.1:c.11438T>A	XP_016865456.1:p.Leu3813Ter
XM_017009968.2:c.11534T>A	XP_016865457.1:p.Leu3845Ter
XM_017009969.2:c.11534T>A	XP_016865458.1:p.Leu3845Ter
XM_017009970.2:c.11534T>A	XP_016865459.1:p.Leu3845Ter
XM_017009971.2:c.11534T>A	XP_016865460.1:p.Leu3845Ter
XM_017009972.1:c.4652T>A	XP_016865461.1:p.Leu1551Ter
XM_017009973.1:c.4631T>A	XP_016865462.1:p.Leu1544Ter
NR_003149.2:n.11529T>A