Canonical Allele Identifier: CA360367478

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050997T>A (hg19) ; chr5:g.90755180T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755180T>A , CM000667.2:g.90755180T>A	GRCh38
NC_000005.9:g.90050997T>A , CM000667.1:g.90050997T>A	GRCh37
NC_000005.8:g.90086753T>A	NCBI36
NG_007083.1:g.201381T>A
NG_007083.2:g.230837T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11575T>A MANE Select	ENSP00000384582.2:p.Leu3859Met
ENST00000425867.3:c.706T>A	ENSP00000392618.3:p.Leu236Met
ENST00000639431.1:c.265+78971T>A	ENSP00000491057.1:n.265+78971T>A
ENST00000640374.1:n.4719T>A
ENST00000640464.1:n.1994T>A
ENST00000405460.6:c.11575T>A	ENSP00000384582.2:p.Leu3859Met
ENST00000509621.1:c.4272T>A
NM_032119.3:c.11575T>A	NP_115495.3:p.Leu3859Met
NR_003149.1:n.11588T>A
XM_011543675.1:c.11572T>A	XP_011541977.1:p.Leu3858Met
XM_011543676.1:c.11494T>A	XP_011541978.1:p.Leu3832Met
XM_011543677.1:c.8878T>A	XP_011541979.1:p.Leu2960Met
XM_011543678.1:c.11575T>A	XP_011541980.1:p.Leu3859Met
NM_032119.4:c.11575T>A MANE Select	NP_115495.3:p.Leu3859Met
XM_017009963.2:c.11596T>A	XP_016865452.1:p.Leu3866Met
XM_017009964.2:c.11593T>A	XP_016865453.1:p.Leu3865Met
XM_017009965.1:c.11593T>A	XP_016865454.1:p.Leu3865Met
XM_017009966.2:c.11515T>A	XP_016865455.1:p.Leu3839Met
XM_017009967.1:c.11500T>A	XP_016865456.1:p.Leu3834Met
XM_017009968.2:c.11596T>A	XP_016865457.1:p.Leu3866Met
XM_017009969.2:c.11596T>A	XP_016865458.1:p.Leu3866Met
XM_017009970.2:c.11596T>A	XP_016865459.1:p.Leu3866Met
XM_017009971.2:c.11596T>A	XP_016865460.1:p.Leu3866Met
XM_017009972.1:c.4714T>A	XP_016865461.1:p.Leu1572Met
XM_017009973.1:c.4693T>A	XP_016865462.1:p.Leu1565Met
NR_003149.2:n.11591T>A