Canonical Allele Identifier: CA445436388

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119248T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823431T>C , CM000667.2:g.90823431T>C	GRCh38
NC_000005.9:g.90119248T>C , CM000667.1:g.90119248T>C	GRCh37
NC_000005.8:g.90155004T>C	NCBI36
NG_007083.1:g.269632T>C
NG_007083.2:g.299088T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16203T>C MANE Select	ENSP00000384582.2:p.Phe5401=
ENST00000425867.3:c.5157T>C	ENSP00000392618.3:p.Phe1719=
ENST00000638510.1:n.3470T>C
ENST00000639431.1:c.265+147222T>C	ENSP00000491057.1:n.265+147222T>C
ENST00000640061.1:n.128+1249T>C
ENST00000640407.1:c.2613T>C	ENSP00000491425.1:p.Phe871=
ENST00000405460.6:c.16203T>C	ENSP00000384582.2:p.Phe5401=
ENST00000425867.2:c.3186T>C	ENSP00000392618.2:p.Phe1062=
NM_032119.3:c.16203T>C	NP_115495.3:p.Phe5401=
NR_003149.1:n.16216T>C
XM_011543675.1:c.16200T>C	XP_011541977.1:p.Phe5400=
XM_011543676.1:c.16122T>C	XP_011541978.1:p.Phe5374=
XM_011543677.1:c.13506T>C	XP_011541979.1:p.Phe4502=
NM_032119.4:c.16203T>C MANE Select	NP_115495.3:p.Phe5401=
XM_017009963.2:c.16224T>C	XP_016865452.1:p.Phe5408=
XM_017009964.2:c.16221T>C	XP_016865453.1:p.Phe5407=
XM_017009965.1:c.16221T>C	XP_016865454.1:p.Phe5407=
XM_017009966.2:c.16143T>C	XP_016865455.1:p.Phe5381=
XM_017009967.1:c.16128T>C	XP_016865456.1:p.Phe5376=
XM_017009968.2:c.16044T>C	XP_016865457.1:p.Phe5348=
XM_017009969.2:c.16224T>C	XP_016865458.1:p.Phe5408=
XM_017009972.1:c.9342T>C	XP_016865461.1:p.Phe3114=
XM_017009973.1:c.9321T>C	XP_016865462.1:p.Phe3107=
NR_003149.2:n.16219T>C