Canonical Allele Identifier: CA360409697

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106555T>G (hg19) ; chr5:g.90810738T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810738T>G , CM000667.2:g.90810738T>G	GRCh38
NC_000005.9:g.90106555T>G , CM000667.1:g.90106555T>G	GRCh37
NC_000005.8:g.90142311T>G	NCBI36
NG_007083.1:g.256939T>G
NG_007083.2:g.286395T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.15478T>G MANE Select	ENSP00000384582.2:p.Tyr5160Asp
ENST00000425867.3:c.4432T>G	ENSP00000392618.3:p.Tyr1478Asp
ENST00000638510.1:n.2745T>G
ENST00000639431.1:c.265+134529T>G	ENSP00000491057.1:n.265+134529T>G
ENST00000640407.1:c.1888T>G	ENSP00000491425.1:p.Tyr630Asp
ENST00000405460.6:c.15478T>G	ENSP00000384582.2:p.Tyr5160Asp
ENST00000425867.2:c.2461T>G	ENSP00000392618.2:p.Tyr821Asp
NM_032119.3:c.15478T>G	NP_115495.3:p.Tyr5160Asp
NR_003149.1:n.15491T>G
XM_011543675.1:c.15475T>G	XP_011541977.1:p.Tyr5159Asp
XM_011543676.1:c.15397T>G	XP_011541978.1:p.Tyr5133Asp
XM_011543677.1:c.12781T>G	XP_011541979.1:p.Tyr4261Asp
NM_032119.4:c.15478T>G MANE Select	NP_115495.3:p.Tyr5160Asp
XM_017009963.2:c.15499T>G	XP_016865452.1:p.Tyr5167Asp
XM_017009964.2:c.15496T>G	XP_016865453.1:p.Tyr5166Asp
XM_017009965.1:c.15496T>G	XP_016865454.1:p.Tyr5166Asp
XM_017009966.2:c.15418T>G	XP_016865455.1:p.Tyr5140Asp
XM_017009967.1:c.15403T>G	XP_016865456.1:p.Tyr5135Asp
XM_017009968.2:c.15319T>G	XP_016865457.1:p.Tyr5107Asp
XM_017009969.2:c.15499T>G	XP_016865458.1:p.Tyr5167Asp
XM_017009971.2:c.*432T>G	XP_016865460.1:n.*432T>G
XM_017009972.1:c.8617T>G	XP_016865461.1:p.Tyr2873Asp
XM_017009973.1:c.8596T>G	XP_016865462.1:p.Tyr2866Asp
NR_003149.2:n.15494T>G