Canonical Allele Identifier: CA445407242

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89913752T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617935T>C , CM000667.2:g.90617935T>C	GRCh38
NC_000005.9:g.89913752T>C , CM000667.1:g.89913752T>C	GRCh37
NC_000005.8:g.89949508T>C	NCBI36
NG_007083.1:g.64136T>C
NG_007083.2:g.93592T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.339T>C MANE Select	ENSP00000384582.2:p.Ile113=
ENST00000638316.1:n.549T>C
ENST00000638638.1:n.746T>C
ENST00000640083.1:n.44T>C
ENST00000640109.1:n.435T>C
ENST00000640281.1:n.398T>C
ENST00000405460.6:c.339T>C	ENSP00000384582.2:p.Ile113=
ENST00000508842.5:c.351T>C	ENSP00000425936.1:p.Ile117=
NM_032119.3:c.339T>C	NP_115495.3:p.Ile113=
NR_003149.1:n.435T>C
XM_011543675.1:c.339T>C	XP_011541977.1:p.Ile113=
XM_011543676.1:c.339T>C	XP_011541978.1:p.Ile113=
XM_011543678.1:c.339T>C	XP_011541980.1:p.Ile113=
XM_011543679.1:c.339T>C	XP_011541981.1:p.Ile113=
NM_032119.4:c.339T>C MANE Select	NP_115495.3:p.Ile113=
XM_017009963.2:c.339T>C	XP_016865452.1:p.Ile113=
XM_017009964.2:c.339T>C	XP_016865453.1:p.Ile113=
XM_017009965.1:c.336T>C	XP_016865454.1:p.Ile112=
XM_017009966.2:c.339T>C	XP_016865455.1:p.Ile113=
XM_017009967.1:c.339T>C	XP_016865456.1:p.Ile113=
XM_017009968.2:c.339T>C	XP_016865457.1:p.Ile113=
XM_017009969.2:c.339T>C	XP_016865458.1:p.Ile113=
XM_017009970.2:c.339T>C	XP_016865459.1:p.Ile113=
XM_017009971.2:c.339T>C	XP_016865460.1:p.Ile113=
XM_017009974.2:c.339T>C	XP_016865463.1:p.Ile113=
NR_003149.2:n.438T>C