Canonical Allele Identifier: CA445412054

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008214T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712397T>C , CM000667.2:g.90712397T>C	GRCh38
NC_000005.9:g.90008214T>C , CM000667.1:g.90008214T>C	GRCh37
NC_000005.8:g.90043970T>C	NCBI36
NG_007083.1:g.158598T>C
NG_007083.2:g.188054T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9153T>C MANE Select	ENSP00000384582.2:p.Ser3051=
ENST00000639431.1:c.265+36188T>C	ENSP00000491057.1:n.265+36188T>C
ENST00000639473.1:n.4612T>C
ENST00000640012.1:c.2960T>C
ENST00000640374.1:n.2297T>C
ENST00000640779.1:c.3882T>C
ENST00000405460.6:c.9153T>C	ENSP00000384582.2:p.Ser3051=
ENST00000509621.1:c.1850T>C
NM_032119.3:c.9153T>C	NP_115495.3:p.Ser3051=
NR_003149.1:n.9166T>C
XM_011543675.1:c.9150T>C	XP_011541977.1:p.Ser3050=
XM_011543676.1:c.9072T>C	XP_011541978.1:p.Ser3024=
XM_011543677.1:c.6456T>C	XP_011541979.1:p.Ser2152=
XM_011543678.1:c.9153T>C	XP_011541980.1:p.Ser3051=
XM_011543679.1:c.9153T>C	XP_011541981.1:p.Ser3051=
XR_948560.1:n.449A>G
NM_032119.4:c.9153T>C MANE Select	NP_115495.3:p.Ser3051=
XM_017009963.2:c.9174T>C	XP_016865452.1:p.Ser3058=
XM_017009964.2:c.9171T>C	XP_016865453.1:p.Ser3057=
XM_017009965.1:c.9171T>C	XP_016865454.1:p.Ser3057=
XM_017009966.2:c.9093T>C	XP_016865455.1:p.Ser3031=
XM_017009967.1:c.9078T>C	XP_016865456.1:p.Ser3026=
XM_017009968.2:c.9174T>C	XP_016865457.1:p.Ser3058=
XM_017009969.2:c.9174T>C	XP_016865458.1:p.Ser3058=
XM_017009970.2:c.9174T>C	XP_016865459.1:p.Ser3058=
XM_017009971.2:c.9174T>C	XP_016865460.1:p.Ser3058=
XM_017009972.1:c.2292T>C	XP_016865461.1:p.Ser764=
XM_017009973.1:c.2271T>C	XP_016865462.1:p.Ser757=
XM_017009974.2:c.9174T>C	XP_016865463.1:p.Ser3058=
NR_003149.2:n.9169T>C