Canonical Allele Identifier: CA360377458

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059165A>G (hg19) ; chr5:g.90763348A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763348A>G , CM000667.2:g.90763348A>G	GRCh38
NC_000005.9:g.90059165A>G , CM000667.1:g.90059165A>G	GRCh37
NC_000005.8:g.90094921A>G	NCBI36
NG_007083.1:g.209549A>G
NG_007083.2:g.239005A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12164A>G MANE Select	ENSP00000384582.2:p.Tyr4055Cys
ENST00000425867.3:c.1118A>G	ENSP00000392618.3:p.Tyr373Cys
ENST00000639431.1:c.265+87139A>G	ENSP00000491057.1:n.265+87139A>G
ENST00000640464.1:n.2583A>G
ENST00000640729.1:n.741A>G
ENST00000405460.6:c.12164A>G	ENSP00000384582.2:p.Tyr4055Cys
NM_032119.3:c.12164A>G	NP_115495.3:p.Tyr4055Cys
NR_003149.1:n.12177A>G
XM_011543675.1:c.12161A>G	XP_011541977.1:p.Tyr4054Cys
XM_011543676.1:c.12083A>G	XP_011541978.1:p.Tyr4028Cys
XM_011543677.1:c.9467A>G	XP_011541979.1:p.Tyr3156Cys
XM_011543678.1:c.12164A>G	XP_011541980.1:p.Tyr4055Cys
NM_032119.4:c.12164A>G MANE Select	NP_115495.3:p.Tyr4055Cys
XM_017009963.2:c.12185A>G	XP_016865452.1:p.Tyr4062Cys
XM_017009964.2:c.12182A>G	XP_016865453.1:p.Tyr4061Cys
XM_017009965.1:c.12182A>G	XP_016865454.1:p.Tyr4061Cys
XM_017009966.2:c.12104A>G	XP_016865455.1:p.Tyr4035Cys
XM_017009967.1:c.12089A>G	XP_016865456.1:p.Tyr4030Cys
XM_017009968.2:c.12185A>G	XP_016865457.1:p.Tyr4062Cys
XM_017009969.2:c.12185A>G	XP_016865458.1:p.Tyr4062Cys
XM_017009970.2:c.12185A>G	XP_016865459.1:p.Tyr4062Cys
XM_017009971.2:c.12185A>G	XP_016865460.1:p.Tyr4062Cys
XM_017009972.1:c.5303A>G	XP_016865461.1:p.Tyr1768Cys
XM_017009973.1:c.5282A>G	XP_016865462.1:p.Tyr1761Cys
NR_003149.2:n.12180A>G