Canonical Allele Identifier: CA360386142

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89913767A>T (hg19) ; chr5:g.90617950A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617950A>T , CM000667.2:g.90617950A>T	GRCh38
NC_000005.9:g.89913767A>T , CM000667.1:g.89913767A>T	GRCh37
NC_000005.8:g.89949523A>T	NCBI36
NG_007083.1:g.64151A>T
NG_007083.2:g.93607A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.354A>T MANE Select	ENSP00000384582.2:p.Leu118Phe
ENST00000638316.1:n.564A>T
ENST00000638638.1:n.761A>T
ENST00000640083.1:n.59A>T
ENST00000640109.1:n.450A>T
ENST00000640281.1:n.413A>T
ENST00000405460.6:c.354A>T	ENSP00000384582.2:p.Leu118Phe
ENST00000508842.5:c.366A>T	ENSP00000425936.1:p.Leu122Phe
NM_032119.3:c.354A>T	NP_115495.3:p.Leu118Phe
NR_003149.1:n.450A>T
XM_011543675.1:c.354A>T	XP_011541977.1:p.Leu118Phe
XM_011543676.1:c.354A>T	XP_011541978.1:p.Leu118Phe
XM_011543678.1:c.354A>T	XP_011541980.1:p.Leu118Phe
XM_011543679.1:c.354A>T	XP_011541981.1:p.Leu118Phe
NM_032119.4:c.354A>T MANE Select	NP_115495.3:p.Leu118Phe
XM_017009963.2:c.354A>T	XP_016865452.1:p.Leu118Phe
XM_017009964.2:c.354A>T	XP_016865453.1:p.Leu118Phe
XM_017009965.1:c.351A>T	XP_016865454.1:p.Leu117Phe
XM_017009966.2:c.354A>T	XP_016865455.1:p.Leu118Phe
XM_017009967.1:c.354A>T	XP_016865456.1:p.Leu118Phe
XM_017009968.2:c.354A>T	XP_016865457.1:p.Leu118Phe
XM_017009969.2:c.354A>T	XP_016865458.1:p.Leu118Phe
XM_017009970.2:c.354A>T	XP_016865459.1:p.Leu118Phe
XM_017009971.2:c.354A>T	XP_016865460.1:p.Leu118Phe
XM_017009974.2:c.354A>T	XP_016865463.1:p.Leu118Phe
NR_003149.2:n.453A>T