Canonical Allele Identifier: CA360407574

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90040892T>A (hg19) ; chr5:g.90745075T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745075T>A , CM000667.2:g.90745075T>A	GRCh38
NC_000005.9:g.90040892T>A , CM000667.1:g.90040892T>A	GRCh37
NC_000005.8:g.90076648T>A	NCBI36
NG_007083.1:g.191276T>A
NG_007083.2:g.220732T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10579T>A MANE Select	ENSP00000384582.2:p.Ser3527Thr
ENST00000639431.1:c.265+68866T>A	ENSP00000491057.1:n.265+68866T>A
ENST00000640374.1:n.3723T>A
ENST00000640464.1:n.998T>A
ENST00000405460.6:c.10579T>A	ENSP00000384582.2:p.Ser3527Thr
ENST00000509621.1:c.3276T>A
NM_032119.3:c.10579T>A	NP_115495.3:p.Ser3527Thr
NR_003149.1:n.10592T>A
XM_011543675.1:c.10576T>A	XP_011541977.1:p.Ser3526Thr
XM_011543676.1:c.10498T>A	XP_011541978.1:p.Ser3500Thr
XM_011543677.1:c.7882T>A	XP_011541979.1:p.Ser2628Thr
XM_011543678.1:c.10579T>A	XP_011541980.1:p.Ser3527Thr
XM_011543679.1:c.10579T>A	XP_011541981.1:p.Ser3527Thr
NM_032119.4:c.10579T>A MANE Select	NP_115495.3:p.Ser3527Thr
XM_017009963.2:c.10600T>A	XP_016865452.1:p.Ser3534Thr
XM_017009964.2:c.10597T>A	XP_016865453.1:p.Ser3533Thr
XM_017009965.1:c.10597T>A	XP_016865454.1:p.Ser3533Thr
XM_017009966.2:c.10519T>A	XP_016865455.1:p.Ser3507Thr
XM_017009967.1:c.10504T>A	XP_016865456.1:p.Ser3502Thr
XM_017009968.2:c.10600T>A	XP_016865457.1:p.Ser3534Thr
XM_017009969.2:c.10600T>A	XP_016865458.1:p.Ser3534Thr
XM_017009970.2:c.10600T>A	XP_016865459.1:p.Ser3534Thr
XM_017009971.2:c.10600T>A	XP_016865460.1:p.Ser3534Thr
XM_017009972.1:c.3718T>A	XP_016865461.1:p.Ser1240Thr
XM_017009973.1:c.3697T>A	XP_016865462.1:p.Ser1233Thr
XM_017009974.2:c.10600T>A	XP_016865463.1:p.Ser3534Thr
NR_003149.2:n.10595T>A