Canonical Allele Identifier: CA138074

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90965478G>T , CM000667.2:g.90965478G>T	GRCh38
NC_000005.9:g.90261295G>T , CM000667.1:g.90261295G>T	GRCh37
NC_000005.8:g.90297051G>T	NCBI36
NG_007083.1:g.411679G>T
NG_007083.2:g.441135G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17920G>T MANE Select	NP_115495.3:p.Ala5974Ser
ENST00000405460.9:c.17920G>T MANE Select	ENSP00000384582.2:p.Ala5974Ser
NM_032119.3:c.17920G>T	NP_115495.3:p.Ala5974Ser
NR_003149.1:n.17933G>T
NR_003149.2:n.17936G>T
ENST00000405460.6:c.17920G>T	ENSP00000384582.2:p.Ala5974Ser
ENST00000425867.2:c.4903G>T	ENSP00000392618.2:p.Ala1635Ser
ENST00000425867.3:c.6874G>T	ENSP00000392618.3:p.Ala2292Ser
ENST00000638510.1:n.5187G>T
ENST00000638990.1:c.1132G>T
ENST00000639431.1:c.266-19866G>T	ENSP00000491057.1:n.266-19866G>T
ENST00000639707.1:c.4G>T	ENSP00000492328.1:p.Ala2Ser
ENST00000639821.1:c.4G>T	ENSP00000492216.1:p.Ala2Ser
ENST00000640369.1:c.4G>T	ENSP00000491401.1:p.Ala2Ser
ENST00000640407.1:c.4369G>T	ENSP00000491425.1:n.4369G>T
ENST00000640815.1:c.4G>T	ENSP00000491767.1:p.Ala2Ser
XM_011543675.1:c.17917G>T	XP_011541977.1:p.Ala5973Ser
XM_011543676.1:c.17839G>T	XP_011541978.1:p.Ala5947Ser
XM_011543677.1:c.15223G>T	XP_011541979.1:p.Ala5075Ser
XM_017009963.2:c.17941G>T	XP_016865452.1:p.Ala5981Ser
XM_017009964.2:c.17938G>T	XP_016865453.1:p.Ala5980Ser
XM_017009965.1:c.17938G>T	XP_016865454.1:p.Ala5980Ser
XM_017009966.2:c.17860G>T	XP_016865455.1:p.Ala5954Ser
XM_017009967.1:c.17845G>T	XP_016865456.1:p.Ala5949Ser
XM_017009968.2:c.17761G>T	XP_016865457.1:p.Ala5921Ser
XM_017009969.2:c.17941G>T	XP_016865458.1:p.Ala5981Ser
XM_017009972.1:c.11059G>T	XP_016865461.1:p.Ala3687Ser
XM_017009973.1:c.11038G>T	XP_016865462.1:p.Ala3680Ser