Canonical Allele Identifier: CA445468381

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106560C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810743C>G , CM000667.2:g.90810743C>G	GRCh38
NC_000005.9:g.90106560C>G , CM000667.1:g.90106560C>G	GRCh37
NC_000005.8:g.90142316C>G	NCBI36
NG_007083.1:g.256944C>G
NG_007083.2:g.286400C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.15483C>G MANE Select	ENSP00000384582.2:p.Leu5161=
ENST00000425867.3:c.4437C>G	ENSP00000392618.3:p.Leu1479=
ENST00000638510.1:n.2750C>G
ENST00000639431.1:c.265+134534C>G	ENSP00000491057.1:n.265+134534C>G
ENST00000640407.1:c.1893C>G	ENSP00000491425.1:p.Leu631=
ENST00000405460.6:c.15483C>G	ENSP00000384582.2:p.Leu5161=
ENST00000425867.2:c.2466C>G	ENSP00000392618.2:p.Leu822=
NM_032119.3:c.15483C>G	NP_115495.3:p.Leu5161=
NR_003149.1:n.15496C>G
XM_011543675.1:c.15480C>G	XP_011541977.1:p.Leu5160=
XM_011543676.1:c.15402C>G	XP_011541978.1:p.Leu5134=
XM_011543677.1:c.12786C>G	XP_011541979.1:p.Leu4262=
NM_032119.4:c.15483C>G MANE Select	NP_115495.3:p.Leu5161=
XM_017009963.2:c.15504C>G	XP_016865452.1:p.Leu5168=
XM_017009964.2:c.15501C>G	XP_016865453.1:p.Leu5167=
XM_017009965.1:c.15501C>G	XP_016865454.1:p.Leu5167=
XM_017009966.2:c.15423C>G	XP_016865455.1:p.Leu5141=
XM_017009967.1:c.15408C>G	XP_016865456.1:p.Leu5136=
XM_017009968.2:c.15324C>G	XP_016865457.1:p.Leu5108=
XM_017009969.2:c.15504C>G	XP_016865458.1:p.Leu5168=
XM_017009971.2:c.*437C>G	XP_016865460.1:n.*437C>G
XM_017009972.1:c.8622C>G	XP_016865461.1:p.Leu2874=
XM_017009973.1:c.8601C>G	XP_016865462.1:p.Leu2867=
NR_003149.2:n.15499C>G