Canonical Allele Identifier: CA445467601

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90087016T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791199T>C , CM000667.2:g.90791199T>C	GRCh38
NC_000005.9:g.90087016T>C , CM000667.1:g.90087016T>C	GRCh37
NC_000005.8:g.90122772T>C	NCBI36
NG_007083.1:g.237400T>C
NG_007083.2:g.266856T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14370T>C MANE Select	ENSP00000384582.2:p.Leu4790=
ENST00000425867.3:c.3324T>C	ENSP00000392618.3:p.Leu1108=
ENST00000507314.2:c.45T>C	ENSP00000491299.1:p.Leu15=
ENST00000638510.1:n.1637T>C
ENST00000638585.1:n.136T>C
ENST00000638975.1:c.999T>C	ENSP00000492630.1:p.Leu333=
ENST00000639431.1:c.265+114990T>C	ENSP00000491057.1:n.265+114990T>C
ENST00000640407.1:c.780T>C	ENSP00000491425.1:p.Leu260=
ENST00000405460.6:c.14370T>C	ENSP00000384582.2:p.Leu4790=
ENST00000425867.2:c.1353T>C	ENSP00000392618.2:p.Leu451=
ENST00000507314.1:n.45T>C
NM_032119.3:c.14370T>C	NP_115495.3:p.Leu4790=
NR_003149.1:n.14383T>C
XM_011543675.1:c.14367T>C	XP_011541977.1:p.Leu4789=
XM_011543676.1:c.14289T>C	XP_011541978.1:p.Leu4763=
XM_011543677.1:c.11673T>C	XP_011541979.1:p.Leu3891=
XM_011543678.1:c.14370T>C	XP_011541980.1:p.Leu4790=
NM_032119.4:c.14370T>C MANE Select	NP_115495.3:p.Leu4790=
XM_017009963.2:c.14391T>C	XP_016865452.1:p.Leu4797=
XM_017009964.2:c.14388T>C	XP_016865453.1:p.Leu4796=
XM_017009965.1:c.14388T>C	XP_016865454.1:p.Leu4796=
XM_017009966.2:c.14310T>C	XP_016865455.1:p.Leu4770=
XM_017009967.1:c.14295T>C	XP_016865456.1:p.Leu4765=
XM_017009968.2:c.14391T>C	XP_016865457.1:p.Leu4797=
XM_017009969.2:c.14391T>C	XP_016865458.1:p.Leu4797=
XM_017009970.2:c.14391T>C	XP_016865459.1:p.Leu4797=
XM_017009971.2:c.14391T>C	XP_016865460.1:p.Leu4797=
XM_017009972.1:c.7509T>C	XP_016865461.1:p.Leu2503=
XM_017009973.1:c.7488T>C	XP_016865462.1:p.Leu2496=
NR_003149.2:n.14386T>C