Canonical Allele Identifier: CA445404510

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988499T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692682T>C , CM000667.2:g.90692682T>C	GRCh38
NC_000005.9:g.89988499T>C , CM000667.1:g.89988499T>C	GRCh37
NC_000005.8:g.90024255T>C	NCBI36
NG_007083.1:g.138883T>C
NG_007083.2:g.168339T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7029T>C MANE Select	ENSP00000384582.2:p.Pro2343=
ENST00000639431.1:c.265+16473T>C	ENSP00000491057.1:n.265+16473T>C
ENST00000639473.1:n.2488T>C
ENST00000640012.1:c.836T>C
ENST00000640374.1:n.173T>C
ENST00000640403.1:c.4320T>C	ENSP00000492531.1:p.Pro1440=
ENST00000640779.1:c.1758T>C
ENST00000405460.6:c.7029T>C	ENSP00000384582.2:p.Pro2343=
NM_032119.3:c.7029T>C	NP_115495.3:p.Pro2343=
NR_003149.1:n.7042T>C
XM_011543675.1:c.7026T>C	XP_011541977.1:p.Pro2342=
XM_011543676.1:c.6948T>C	XP_011541978.1:p.Pro2316=
XM_011543677.1:c.4332T>C	XP_011541979.1:p.Pro1444=
XM_011543678.1:c.7029T>C	XP_011541980.1:p.Pro2343=
XM_011543679.1:c.7029T>C	XP_011541981.1:p.Pro2343=
NM_032119.4:c.7029T>C MANE Select	NP_115495.3:p.Pro2343=
XM_017009963.2:c.7029T>C	XP_016865452.1:p.Pro2343=
XM_017009964.2:c.7026T>C	XP_016865453.1:p.Pro2342=
XM_017009965.1:c.7026T>C	XP_016865454.1:p.Pro2342=
XM_017009966.2:c.6948T>C	XP_016865455.1:p.Pro2316=
XM_017009967.1:c.6933T>C	XP_016865456.1:p.Pro2311=
XM_017009968.2:c.7029T>C	XP_016865457.1:p.Pro2343=
XM_017009969.2:c.7029T>C	XP_016865458.1:p.Pro2343=
XM_017009970.2:c.7029T>C	XP_016865459.1:p.Pro2343=
XM_017009971.2:c.7029T>C	XP_016865460.1:p.Pro2343=
XM_017009972.1:c.147T>C	XP_016865461.1:p.Pro49=
XM_017009973.1:c.147T>C	XP_016865462.1:p.Pro49=
XM_017009974.2:c.7029T>C	XP_016865463.1:p.Pro2343=
NR_003149.2:n.7045T>C