Canonical Allele Identifier: CA360365646

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89923103A>C (hg19) ; chr5:g.90627286A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627286A>C , CM000667.2:g.90627286A>C	GRCh38
NC_000005.9:g.89923103A>C , CM000667.1:g.89923103A>C	GRCh37
NC_000005.8:g.89958859A>C	NCBI36
NG_007083.1:g.73487A>C
NG_007083.2:g.102943A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.748A>C MANE Select	ENSP00000384582.2:p.Asn250His
ENST00000640083.1:n.453A>C
ENST00000640109.1:n.844A>C
ENST00000640281.1:n.807A>C
ENST00000405460.6:c.748A>C	ENSP00000384582.2:p.Asn250His
NM_032119.3:c.748A>C	NP_115495.3:p.Asn250His
NR_003149.1:n.844A>C
XM_011543675.1:c.748A>C	XP_011541977.1:p.Asn250His
XM_011543676.1:c.748A>C	XP_011541978.1:p.Asn250His
XM_011543678.1:c.748A>C	XP_011541980.1:p.Asn250His
XM_011543679.1:c.748A>C	XP_011541981.1:p.Asn250His
NM_032119.4:c.748A>C MANE Select	NP_115495.3:p.Asn250His
XM_017009963.2:c.748A>C	XP_016865452.1:p.Asn250His
XM_017009964.2:c.748A>C	XP_016865453.1:p.Asn250His
XM_017009965.1:c.745A>C	XP_016865454.1:p.Asn249His
XM_017009966.2:c.748A>C	XP_016865455.1:p.Asn250His
XM_017009967.1:c.652A>C	XP_016865456.1:p.Asn218His
XM_017009968.2:c.748A>C	XP_016865457.1:p.Asn250His
XM_017009969.2:c.748A>C	XP_016865458.1:p.Asn250His
XM_017009970.2:c.748A>C	XP_016865459.1:p.Asn250His
XM_017009971.2:c.748A>C	XP_016865460.1:p.Asn250His
XM_017009974.2:c.748A>C	XP_016865463.1:p.Asn250His
NR_003149.2:n.847A>C