Canonical Allele Identifier: CA445467966

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106716T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810899T>C , CM000667.2:g.90810899T>C	GRCh38
NC_000005.9:g.90106716T>C , CM000667.1:g.90106716T>C	GRCh37
NC_000005.8:g.90142472T>C	NCBI36
NG_007083.1:g.257100T>C
NG_007083.2:g.286556T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15639T>C MANE Select	ENSP00000384582.2:p.Asn5213=
ENST00000425867.3:c.4593T>C	ENSP00000392618.3:p.Asn1531=
ENST00000638510.1:n.2906T>C
ENST00000639431.1:c.265+134690T>C	ENSP00000491057.1:n.265+134690T>C
ENST00000640407.1:c.2049T>C	ENSP00000491425.1:p.Asn683=
ENST00000405460.6:c.15639T>C	ENSP00000384582.2:p.Asn5213=
ENST00000425867.2:c.2622T>C	ENSP00000392618.2:p.Asn874=
NM_032119.3:c.15639T>C	NP_115495.3:p.Asn5213=
NR_003149.1:n.15652T>C
XM_011543675.1:c.15636T>C	XP_011541977.1:p.Asn5212=
XM_011543676.1:c.15558T>C	XP_011541978.1:p.Asn5186=
XM_011543677.1:c.12942T>C	XP_011541979.1:p.Asn4314=
NM_032119.4:c.15639T>C MANE Select	NP_115495.3:p.Asn5213=
XM_017009963.2:c.15660T>C	XP_016865452.1:p.Asn5220=
XM_017009964.2:c.15657T>C	XP_016865453.1:p.Asn5219=
XM_017009965.1:c.15657T>C	XP_016865454.1:p.Asn5219=
XM_017009966.2:c.15579T>C	XP_016865455.1:p.Asn5193=
XM_017009967.1:c.15564T>C	XP_016865456.1:p.Asn5188=
XM_017009968.2:c.15480T>C	XP_016865457.1:p.Asn5160=
XM_017009969.2:c.15660T>C	XP_016865458.1:p.Asn5220=
XM_017009972.1:c.8778T>C	XP_016865461.1:p.Asn2926=
XM_017009973.1:c.8757T>C	XP_016865462.1:p.Asn2919=
NR_003149.2:n.15655T>C