Canonical Allele Identifier: CA360384820

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89913622T>A (hg19) ; chr5:g.90617805T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617805T>A , CM000667.2:g.90617805T>A	GRCh38
NC_000005.9:g.89913622T>A , CM000667.1:g.89913622T>A	GRCh37
NC_000005.8:g.89949378T>A	NCBI36
NG_007083.1:g.64006T>A
NG_007083.2:g.93462T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.209T>A MANE Select	ENSP00000384582.2:p.Leu70Gln
ENST00000638316.1:n.419T>A
ENST00000638638.1:n.616T>A
ENST00000640109.1:n.305T>A
ENST00000640281.1:n.268T>A
ENST00000405460.6:c.209T>A	ENSP00000384582.2:p.Leu70Gln
ENST00000508842.5:c.221T>A	ENSP00000425936.1:p.Leu74Gln
NM_032119.3:c.209T>A	NP_115495.3:p.Leu70Gln
NR_003149.1:n.305T>A
XM_011543675.1:c.209T>A	XP_011541977.1:p.Leu70Gln
XM_011543676.1:c.209T>A	XP_011541978.1:p.Leu70Gln
XM_011543678.1:c.209T>A	XP_011541980.1:p.Leu70Gln
XM_011543679.1:c.209T>A	XP_011541981.1:p.Leu70Gln
NM_032119.4:c.209T>A MANE Select	NP_115495.3:p.Leu70Gln
XM_017009963.2:c.209T>A	XP_016865452.1:p.Leu70Gln
XM_017009964.2:c.209T>A	XP_016865453.1:p.Leu70Gln
XM_017009965.1:c.206T>A	XP_016865454.1:p.Leu69Gln
XM_017009966.2:c.209T>A	XP_016865455.1:p.Leu70Gln
XM_017009967.1:c.209T>A	XP_016865456.1:p.Leu70Gln
XM_017009968.2:c.209T>A	XP_016865457.1:p.Leu70Gln
XM_017009969.2:c.209T>A	XP_016865458.1:p.Leu70Gln
XM_017009970.2:c.209T>A	XP_016865459.1:p.Leu70Gln
XM_017009971.2:c.209T>A	XP_016865460.1:p.Leu70Gln
XM_017009974.2:c.209T>A	XP_016865463.1:p.Leu70Gln
NR_003149.2:n.308T>A