Canonical Allele Identifier: CA445416101

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041483A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745666A>C , CM000667.2:g.90745666A>C	GRCh38
NC_000005.9:g.90041483A>C , CM000667.1:g.90041483A>C	GRCh37
NC_000005.8:g.90077239A>C	NCBI36
NG_007083.1:g.191867A>C
NG_007083.2:g.221323A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10845A>C MANE Select	ENSP00000384582.2:p.Pro3615=
ENST00000639431.1:c.265+69457A>C	ENSP00000491057.1:n.265+69457A>C
ENST00000640374.1:n.3989A>C
ENST00000640464.1:n.1264A>C
ENST00000405460.6:c.10845A>C	ENSP00000384582.2:p.Pro3615=
ENST00000509621.1:c.3542A>C
NM_032119.3:c.10845A>C	NP_115495.3:p.Pro3615=
NR_003149.1:n.10858A>C
XM_011543675.1:c.10842A>C	XP_011541977.1:p.Pro3614=
XM_011543676.1:c.10764A>C	XP_011541978.1:p.Pro3588=
XM_011543677.1:c.8148A>C	XP_011541979.1:p.Pro2716=
XM_011543678.1:c.10845A>C	XP_011541980.1:p.Pro3615=
XM_011543679.1:c.*67A>C	XP_011541981.1:n.*67A>C
NM_032119.4:c.10845A>C MANE Select	NP_115495.3:p.Pro3615=
XM_017009963.2:c.10866A>C	XP_016865452.1:p.Pro3622=
XM_017009964.2:c.10863A>C	XP_016865453.1:p.Pro3621=
XM_017009965.1:c.10863A>C	XP_016865454.1:p.Pro3621=
XM_017009966.2:c.10785A>C	XP_016865455.1:p.Pro3595=
XM_017009967.1:c.10770A>C	XP_016865456.1:p.Pro3590=
XM_017009968.2:c.10866A>C	XP_016865457.1:p.Pro3622=
XM_017009969.2:c.10866A>C	XP_016865458.1:p.Pro3622=
XM_017009970.2:c.10866A>C	XP_016865459.1:p.Pro3622=
XM_017009971.2:c.10866A>C	XP_016865460.1:p.Pro3622=
XM_017009972.1:c.3984A>C	XP_016865461.1:p.Pro1328=
XM_017009973.1:c.3963A>C	XP_016865462.1:p.Pro1321=
XM_017009974.2:c.*67A>C	XP_016865463.1:n.*67A>C
NR_003149.2:n.10861A>C