Canonical Allele Identifier: CA360425657

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119352C>A (hg19) ; chr5:g.90823535C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823535C>A , CM000667.2:g.90823535C>A	GRCh38
NC_000005.9:g.90119352C>A , CM000667.1:g.90119352C>A	GRCh37
NC_000005.8:g.90155108C>A	NCBI36
NG_007083.1:g.269736C>A
NG_007083.2:g.299192C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16307C>A MANE Select	ENSP00000384582.2:p.Thr5436Asn
ENST00000425867.3:c.5261C>A	ENSP00000392618.3:p.Thr1754Asn
ENST00000638510.1:n.3574C>A
ENST00000639431.1:c.265+147326C>A	ENSP00000491057.1:n.265+147326C>A
ENST00000640061.1:n.128+1353C>A
ENST00000640407.1:c.2717C>A	ENSP00000491425.1:p.Thr906Asn
ENST00000405460.6:c.16307C>A	ENSP00000384582.2:p.Thr5436Asn
ENST00000425867.2:c.3290C>A	ENSP00000392618.2:p.Thr1097Asn
NM_032119.3:c.16307C>A	NP_115495.3:p.Thr5436Asn
NR_003149.1:n.16320C>A
XM_011543675.1:c.16304C>A	XP_011541977.1:p.Thr5435Asn
XM_011543676.1:c.16226C>A	XP_011541978.1:p.Thr5409Asn
XM_011543677.1:c.13610C>A	XP_011541979.1:p.Thr4537Asn
NM_032119.4:c.16307C>A MANE Select	NP_115495.3:p.Thr5436Asn
XM_017009963.2:c.16328C>A	XP_016865452.1:p.Thr5443Asn
XM_017009964.2:c.16325C>A	XP_016865453.1:p.Thr5442Asn
XM_017009965.1:c.16325C>A	XP_016865454.1:p.Thr5442Asn
XM_017009966.2:c.16247C>A	XP_016865455.1:p.Thr5416Asn
XM_017009967.1:c.16232C>A	XP_016865456.1:p.Thr5411Asn
XM_017009968.2:c.16148C>A	XP_016865457.1:p.Thr5383Asn
XM_017009969.2:c.16328C>A	XP_016865458.1:p.Thr5443Asn
XM_017009972.1:c.9446C>A	XP_016865461.1:p.Thr3149Asn
XM_017009973.1:c.9425C>A	XP_016865462.1:p.Thr3142Asn
NR_003149.2:n.16323C>A