Canonical Allele Identifier: CA360370938

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988462C>A (hg19) ; chr5:g.90692645C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692645C>A , CM000667.2:g.90692645C>A	GRCh38
NC_000005.9:g.89988462C>A , CM000667.1:g.89988462C>A	GRCh37
NC_000005.8:g.90024218C>A	NCBI36
NG_007083.1:g.138846C>A
NG_007083.2:g.168302C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6992C>A MANE Select	ENSP00000384582.2:p.Thr2331Asn
ENST00000639431.1:c.265+16436C>A	ENSP00000491057.1:n.265+16436C>A
ENST00000639473.1:n.2451C>A
ENST00000640012.1:c.799C>A
ENST00000640374.1:n.136C>A
ENST00000640403.1:c.4283C>A	ENSP00000492531.1:p.Thr1428Asn
ENST00000640779.1:c.1721C>A
ENST00000405460.6:c.6992C>A	ENSP00000384582.2:p.Thr2331Asn
NM_032119.3:c.6992C>A	NP_115495.3:p.Thr2331Asn
NR_003149.1:n.7005C>A
XM_011543675.1:c.6989C>A	XP_011541977.1:p.Thr2330Asn
XM_011543676.1:c.6911C>A	XP_011541978.1:p.Thr2304Asn
XM_011543677.1:c.4295C>A	XP_011541979.1:p.Thr1432Asn
XM_011543678.1:c.6992C>A	XP_011541980.1:p.Thr2331Asn
XM_011543679.1:c.6992C>A	XP_011541981.1:p.Thr2331Asn
NM_032119.4:c.6992C>A MANE Select	NP_115495.3:p.Thr2331Asn
XM_017009963.2:c.6992C>A	XP_016865452.1:p.Thr2331Asn
XM_017009964.2:c.6989C>A	XP_016865453.1:p.Thr2330Asn
XM_017009965.1:c.6989C>A	XP_016865454.1:p.Thr2330Asn
XM_017009966.2:c.6911C>A	XP_016865455.1:p.Thr2304Asn
XM_017009967.1:c.6896C>A	XP_016865456.1:p.Thr2299Asn
XM_017009968.2:c.6992C>A	XP_016865457.1:p.Thr2331Asn
XM_017009969.2:c.6992C>A	XP_016865458.1:p.Thr2331Asn
XM_017009970.2:c.6992C>A	XP_016865459.1:p.Thr2331Asn
XM_017009971.2:c.6992C>A	XP_016865460.1:p.Thr2331Asn
XM_017009972.1:c.110C>A	XP_016865461.1:p.Thr37Asn
XM_017009973.1:c.110C>A	XP_016865462.1:p.Thr37Asn
XM_017009974.2:c.6992C>A	XP_016865463.1:p.Thr2331Asn
NR_003149.2:n.7008C>A