Canonical Allele Identifier: CA360366825

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050905A>C (hg19) ; chr5:g.90755088A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755088A>C , CM000667.2:g.90755088A>C	GRCh38
NC_000005.9:g.90050905A>C , CM000667.1:g.90050905A>C	GRCh37
NC_000005.8:g.90086661A>C	NCBI36
NG_007083.1:g.201289A>C
NG_007083.2:g.230745A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11483A>C MANE Select	ENSP00000384582.2:p.Asn3828Thr
ENST00000425867.3:c.614A>C	ENSP00000392618.3:p.Asn205Thr
ENST00000639431.1:c.265+78879A>C	ENSP00000491057.1:n.265+78879A>C
ENST00000640374.1:n.4627A>C
ENST00000640464.1:n.1902A>C
ENST00000405460.6:c.11483A>C	ENSP00000384582.2:p.Asn3828Thr
ENST00000509621.1:c.4180A>C
NM_032119.3:c.11483A>C	NP_115495.3:p.Asn3828Thr
NR_003149.1:n.11496A>C
XM_011543675.1:c.11480A>C	XP_011541977.1:p.Asn3827Thr
XM_011543676.1:c.11402A>C	XP_011541978.1:p.Asn3801Thr
XM_011543677.1:c.8786A>C	XP_011541979.1:p.Asn2929Thr
XM_011543678.1:c.11483A>C	XP_011541980.1:p.Asn3828Thr
NM_032119.4:c.11483A>C MANE Select	NP_115495.3:p.Asn3828Thr
XM_017009963.2:c.11504A>C	XP_016865452.1:p.Asn3835Thr
XM_017009964.2:c.11501A>C	XP_016865453.1:p.Asn3834Thr
XM_017009965.1:c.11501A>C	XP_016865454.1:p.Asn3834Thr
XM_017009966.2:c.11423A>C	XP_016865455.1:p.Asn3808Thr
XM_017009967.1:c.11408A>C	XP_016865456.1:p.Asn3803Thr
XM_017009968.2:c.11504A>C	XP_016865457.1:p.Asn3835Thr
XM_017009969.2:c.11504A>C	XP_016865458.1:p.Asn3835Thr
XM_017009970.2:c.11504A>C	XP_016865459.1:p.Asn3835Thr
XM_017009971.2:c.11504A>C	XP_016865460.1:p.Asn3835Thr
XM_017009972.1:c.4622A>C	XP_016865461.1:p.Asn1541Thr
XM_017009973.1:c.4601A>C	XP_016865462.1:p.Asn1534Thr
NR_003149.2:n.11499A>C