Canonical Allele Identifier: CA360397579

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012475T>A (hg19) ; chr5:g.90716658T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716658T>A , CM000667.2:g.90716658T>A	GRCh38
NC_000005.9:g.90012475T>A , CM000667.1:g.90012475T>A	GRCh37
NC_000005.8:g.90048231T>A	NCBI36
NG_007083.1:g.162859T>A
NG_007083.2:g.192315T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9376T>A MANE Select	ENSP00000384582.2:p.Ser3126Thr
ENST00000639431.1:c.265+40449T>A	ENSP00000491057.1:n.265+40449T>A
ENST00000639473.1:n.4835T>A
ENST00000640012.1:c.3183T>A
ENST00000640374.1:n.2520T>A
ENST00000640779.1:c.4105T>A
ENST00000405460.6:c.9376T>A	ENSP00000384582.2:p.Ser3126Thr
ENST00000509621.1:c.2073T>A
NM_032119.3:c.9376T>A	NP_115495.3:p.Ser3126Thr
NR_003149.1:n.9389T>A
XM_011543675.1:c.9373T>A	XP_011541977.1:p.Ser3125Thr
XM_011543676.1:c.9295T>A	XP_011541978.1:p.Ser3099Thr
XM_011543677.1:c.6679T>A	XP_011541979.1:p.Ser2227Thr
XM_011543678.1:c.9376T>A	XP_011541980.1:p.Ser3126Thr
XM_011543679.1:c.9376T>A	XP_011541981.1:p.Ser3126Thr
XR_948560.1:n.272-849A>T
NM_032119.4:c.9376T>A MANE Select	NP_115495.3:p.Ser3126Thr
XM_017009963.2:c.9397T>A	XP_016865452.1:p.Ser3133Thr
XM_017009964.2:c.9394T>A	XP_016865453.1:p.Ser3132Thr
XM_017009965.1:c.9394T>A	XP_016865454.1:p.Ser3132Thr
XM_017009966.2:c.9316T>A	XP_016865455.1:p.Ser3106Thr
XM_017009967.1:c.9301T>A	XP_016865456.1:p.Ser3101Thr
XM_017009968.2:c.9397T>A	XP_016865457.1:p.Ser3133Thr
XM_017009969.2:c.9397T>A	XP_016865458.1:p.Ser3133Thr
XM_017009970.2:c.9397T>A	XP_016865459.1:p.Ser3133Thr
XM_017009971.2:c.9397T>A	XP_016865460.1:p.Ser3133Thr
XM_017009972.1:c.2515T>A	XP_016865461.1:p.Ser839Thr
XM_017009973.1:c.2494T>A	XP_016865462.1:p.Ser832Thr
XM_017009974.2:c.9397T>A	XP_016865463.1:p.Ser3133Thr
XR_001742802.1:n.2523-849A>T
NR_003149.2:n.9392T>A