Canonical Allele Identifier: CA360388772

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89999506T>C (hg19) ; chr5:g.90703689T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90703689T>C , CM000667.2:g.90703689T>C	GRCh38
NC_000005.9:g.89999506T>C , CM000667.1:g.89999506T>C	GRCh37
NC_000005.8:g.90035262T>C	NCBI36
NG_007083.1:g.149890T>C
NG_007083.2:g.179346T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.8180T>C MANE Select	ENSP00000384582.2:p.Ile2727Thr
ENST00000639431.1:c.265+27480T>C	ENSP00000491057.1:n.265+27480T>C
ENST00000639473.1:n.3639T>C
ENST00000640012.1:c.1987T>C
ENST00000640374.1:n.1324T>C
ENST00000640403.1:c.5471T>C	ENSP00000492531.1:p.Ile1824Thr
ENST00000640779.1:c.2909T>C
ENST00000405460.6:c.8180T>C	ENSP00000384582.2:p.Ile2727Thr
ENST00000509621.1:c.877T>C
NM_032119.3:c.8180T>C	NP_115495.3:p.Ile2727Thr
NR_003149.1:n.8193T>C
XM_011543675.1:c.8177T>C	XP_011541977.1:p.Ile2726Thr
XM_011543676.1:c.8099T>C	XP_011541978.1:p.Ile2700Thr
XM_011543677.1:c.5483T>C	XP_011541979.1:p.Ile1828Thr
XM_011543678.1:c.8180T>C	XP_011541980.1:p.Ile2727Thr
XM_011543679.1:c.8180T>C	XP_011541981.1:p.Ile2727Thr
NM_032119.4:c.8180T>C MANE Select	NP_115495.3:p.Ile2727Thr
XM_017009963.2:c.8180T>C	XP_016865452.1:p.Ile2727Thr
XM_017009964.2:c.8177T>C	XP_016865453.1:p.Ile2726Thr
XM_017009965.1:c.8177T>C	XP_016865454.1:p.Ile2726Thr
XM_017009966.2:c.8099T>C	XP_016865455.1:p.Ile2700Thr
XM_017009967.1:c.8084T>C	XP_016865456.1:p.Ile2695Thr
XM_017009968.2:c.8180T>C	XP_016865457.1:p.Ile2727Thr
XM_017009969.2:c.8180T>C	XP_016865458.1:p.Ile2727Thr
XM_017009970.2:c.8180T>C	XP_016865459.1:p.Ile2727Thr
XM_017009971.2:c.8180T>C	XP_016865460.1:p.Ile2727Thr
XM_017009972.1:c.1298T>C	XP_016865461.1:p.Ile433Thr
XM_017009973.1:c.1298T>C	XP_016865462.1:p.Ile433Thr
XM_017009974.2:c.8180T>C	XP_016865463.1:p.Ile2727Thr
NR_003149.2:n.8196T>C