Canonical Allele Identifier: CA360426908

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90261322T>G (hg19) ; chr5:g.90965505T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90965505T>G , CM000667.2:g.90965505T>G	GRCh38
NC_000005.9:g.90261322T>G , CM000667.1:g.90261322T>G	GRCh37
NC_000005.8:g.90297078T>G	NCBI36
NG_007083.1:g.411706T>G
NG_007083.2:g.441162T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.17947T>G MANE Select	ENSP00000384582.2:p.Cys5983Gly
ENST00000425867.3:c.6901T>G	ENSP00000392618.3:p.Cys2301Gly
ENST00000638510.1:n.5214T>G
ENST00000638990.1:c.1159T>G
ENST00000639431.1:c.266-19839T>G	ENSP00000491057.1:n.266-19839T>G
ENST00000639707.1:c.31T>G	ENSP00000492328.1:p.Cys11Gly
ENST00000639821.1:c.31T>G	ENSP00000492216.1:p.Cys11Gly
ENST00000640369.1:c.31T>G	ENSP00000491401.1:p.Cys11Gly
ENST00000640407.1:c.4396T>G	ENSP00000491425.1:n.4396T>G
ENST00000640815.1:c.31T>G	ENSP00000491767.1:p.Cys11Gly
ENST00000405460.6:c.17947T>G	ENSP00000384582.2:p.Cys5983Gly
ENST00000425867.2:c.4930T>G	ENSP00000392618.2:p.Cys1644Gly
NM_032119.3:c.17947T>G	NP_115495.3:p.Cys5983Gly
NR_003149.1:n.17960T>G
XM_011543675.1:c.17944T>G	XP_011541977.1:p.Cys5982Gly
XM_011543676.1:c.17866T>G	XP_011541978.1:p.Cys5956Gly
XM_011543677.1:c.15250T>G	XP_011541979.1:p.Cys5084Gly
NM_032119.4:c.17947T>G MANE Select	NP_115495.3:p.Cys5983Gly
XM_017009963.2:c.17968T>G	XP_016865452.1:p.Cys5990Gly
XM_017009964.2:c.17965T>G	XP_016865453.1:p.Cys5989Gly
XM_017009965.1:c.17965T>G	XP_016865454.1:p.Cys5989Gly
XM_017009966.2:c.17887T>G	XP_016865455.1:p.Cys5963Gly
XM_017009967.1:c.17872T>G	XP_016865456.1:p.Cys5958Gly
XM_017009968.2:c.17788T>G	XP_016865457.1:p.Cys5930Gly
XM_017009969.2:c.17968T>G	XP_016865458.1:p.Cys5990Gly
XM_017009972.1:c.11086T>G	XP_016865461.1:p.Cys3696Gly
XM_017009973.1:c.11065T>G	XP_016865462.1:p.Cys3689Gly
NR_003149.2:n.17963T>G