Canonical Allele Identifier: CA445467979

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106722C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810905C>A , CM000667.2:g.90810905C>A	GRCh38
NC_000005.9:g.90106722C>A , CM000667.1:g.90106722C>A	GRCh37
NC_000005.8:g.90142478C>A	NCBI36
NG_007083.1:g.257106C>A
NG_007083.2:g.286562C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15645C>A MANE Select	ENSP00000384582.2:p.Ser5215=
ENST00000425867.3:c.4599C>A	ENSP00000392618.3:p.Ser1533=
ENST00000638510.1:n.2912C>A
ENST00000639431.1:c.265+134696C>A	ENSP00000491057.1:n.265+134696C>A
ENST00000640407.1:c.2055C>A	ENSP00000491425.1:p.Ser685=
ENST00000405460.6:c.15645C>A	ENSP00000384582.2:p.Ser5215=
ENST00000425867.2:c.2628C>A	ENSP00000392618.2:p.Ser876=
NM_032119.3:c.15645C>A	NP_115495.3:p.Ser5215=
NR_003149.1:n.15658C>A
XM_011543675.1:c.15642C>A	XP_011541977.1:p.Ser5214=
XM_011543676.1:c.15564C>A	XP_011541978.1:p.Ser5188=
XM_011543677.1:c.12948C>A	XP_011541979.1:p.Ser4316=
NM_032119.4:c.15645C>A MANE Select	NP_115495.3:p.Ser5215=
XM_017009963.2:c.15666C>A	XP_016865452.1:p.Ser5222=
XM_017009964.2:c.15663C>A	XP_016865453.1:p.Ser5221=
XM_017009965.1:c.15663C>A	XP_016865454.1:p.Ser5221=
XM_017009966.2:c.15585C>A	XP_016865455.1:p.Ser5195=
XM_017009967.1:c.15570C>A	XP_016865456.1:p.Ser5190=
XM_017009968.2:c.15486C>A	XP_016865457.1:p.Ser5162=
XM_017009969.2:c.15666C>A	XP_016865458.1:p.Ser5222=
XM_017009972.1:c.8784C>A	XP_016865461.1:p.Ser2928=
XM_017009973.1:c.8763C>A	XP_016865462.1:p.Ser2921=
NR_003149.2:n.15661C>A