Canonical Allele Identifier: CA360409704

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106556A>G (hg19) ; chr5:g.90810739A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810739A>G , CM000667.2:g.90810739A>G	GRCh38
NC_000005.9:g.90106556A>G , CM000667.1:g.90106556A>G	GRCh37
NC_000005.8:g.90142312A>G	NCBI36
NG_007083.1:g.256940A>G
NG_007083.2:g.286396A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.15479A>G MANE Select	ENSP00000384582.2:p.Tyr5160Cys
ENST00000425867.3:c.4433A>G	ENSP00000392618.3:p.Tyr1478Cys
ENST00000638510.1:n.2746A>G
ENST00000639431.1:c.265+134530A>G	ENSP00000491057.1:n.265+134530A>G
ENST00000640407.1:c.1889A>G	ENSP00000491425.1:p.Tyr630Cys
ENST00000405460.6:c.15479A>G	ENSP00000384582.2:p.Tyr5160Cys
ENST00000425867.2:c.2462A>G	ENSP00000392618.2:p.Tyr821Cys
NM_032119.3:c.15479A>G	NP_115495.3:p.Tyr5160Cys
NR_003149.1:n.15492A>G
XM_011543675.1:c.15476A>G	XP_011541977.1:p.Tyr5159Cys
XM_011543676.1:c.15398A>G	XP_011541978.1:p.Tyr5133Cys
XM_011543677.1:c.12782A>G	XP_011541979.1:p.Tyr4261Cys
NM_032119.4:c.15479A>G MANE Select	NP_115495.3:p.Tyr5160Cys
XM_017009963.2:c.15500A>G	XP_016865452.1:p.Tyr5167Cys
XM_017009964.2:c.15497A>G	XP_016865453.1:p.Tyr5166Cys
XM_017009965.1:c.15497A>G	XP_016865454.1:p.Tyr5166Cys
XM_017009966.2:c.15419A>G	XP_016865455.1:p.Tyr5140Cys
XM_017009967.1:c.15404A>G	XP_016865456.1:p.Tyr5135Cys
XM_017009968.2:c.15320A>G	XP_016865457.1:p.Tyr5107Cys
XM_017009969.2:c.15500A>G	XP_016865458.1:p.Tyr5167Cys
XM_017009971.2:c.*433A>G	XP_016865460.1:n.*433A>G
XM_017009972.1:c.8618A>G	XP_016865461.1:p.Tyr2873Cys
XM_017009973.1:c.8597A>G	XP_016865462.1:p.Tyr2866Cys
NR_003149.2:n.15495A>G