Canonical Allele Identifier: CA360398971

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90085616T>C (hg19) ; chr5:g.90789799T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789799T>C , CM000667.2:g.90789799T>C	GRCh38
NC_000005.9:g.90085616T>C , CM000667.1:g.90085616T>C	GRCh37
NC_000005.8:g.90121372T>C	NCBI36
NG_007083.1:g.236000T>C
NG_007083.2:g.265456T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.13991T>C MANE Select	ENSP00000384582.2:p.Leu4664Pro
ENST00000425867.3:c.2945T>C	ENSP00000392618.3:p.Leu982Pro
ENST00000638510.1:n.1258T>C
ENST00000638975.1:c.620T>C	ENSP00000492630.1:p.Leu207Pro
ENST00000639431.1:c.265+113590T>C	ENSP00000491057.1:n.265+113590T>C
ENST00000640407.1:c.401T>C	ENSP00000491425.1:p.Leu134Pro
ENST00000405460.6:c.13991T>C	ENSP00000384582.2:p.Leu4664Pro
ENST00000425867.2:c.974T>C	ENSP00000392618.2:p.Leu325Pro
NM_032119.3:c.13991T>C	NP_115495.3:p.Leu4664Pro
NR_003149.1:n.14004T>C
XM_011543675.1:c.13988T>C	XP_011541977.1:p.Leu4663Pro
XM_011543676.1:c.13910T>C	XP_011541978.1:p.Leu4637Pro
XM_011543677.1:c.11294T>C	XP_011541979.1:p.Leu3765Pro
XM_011543678.1:c.13991T>C	XP_011541980.1:p.Leu4664Pro
NM_032119.4:c.13991T>C MANE Select	NP_115495.3:p.Leu4664Pro
XM_017009963.2:c.14012T>C	XP_016865452.1:p.Leu4671Pro
XM_017009964.2:c.14009T>C	XP_016865453.1:p.Leu4670Pro
XM_017009965.1:c.14009T>C	XP_016865454.1:p.Leu4670Pro
XM_017009966.2:c.13931T>C	XP_016865455.1:p.Leu4644Pro
XM_017009967.1:c.13916T>C	XP_016865456.1:p.Leu4639Pro
XM_017009968.2:c.14012T>C	XP_016865457.1:p.Leu4671Pro
XM_017009969.2:c.14012T>C	XP_016865458.1:p.Leu4671Pro
XM_017009970.2:c.14012T>C	XP_016865459.1:p.Leu4671Pro
XM_017009971.2:c.14012T>C	XP_016865460.1:p.Leu4671Pro
XM_017009972.1:c.7130T>C	XP_016865461.1:p.Leu2377Pro
XM_017009973.1:c.7109T>C	XP_016865462.1:p.Leu2370Pro
NR_003149.2:n.14007T>C