Canonical Allele Identifier: CA360398760

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90085573T>G (hg19) ; chr5:g.90789756T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789756T>G , CM000667.2:g.90789756T>G	GRCh38
NC_000005.9:g.90085573T>G , CM000667.1:g.90085573T>G	GRCh37
NC_000005.8:g.90121329T>G	NCBI36
NG_007083.1:g.235957T>G
NG_007083.2:g.265413T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.13948T>G MANE Select	ENSP00000384582.2:p.Ser4650Ala
ENST00000425867.3:c.2902T>G	ENSP00000392618.3:p.Ser968Ala
ENST00000638510.1:n.1215T>G
ENST00000638975.1:c.577T>G	ENSP00000492630.1:p.Ser193Ala
ENST00000639431.1:c.265+113547T>G	ENSP00000491057.1:n.265+113547T>G
ENST00000640407.1:c.358T>G	ENSP00000491425.1:p.Ser120Ala
ENST00000405460.6:c.13948T>G	ENSP00000384582.2:p.Ser4650Ala
ENST00000425867.2:c.931T>G	ENSP00000392618.2:p.Ser311Ala
NM_032119.3:c.13948T>G	NP_115495.3:p.Ser4650Ala
NR_003149.1:n.13961T>G
XM_011543675.1:c.13945T>G	XP_011541977.1:p.Ser4649Ala
XM_011543676.1:c.13867T>G	XP_011541978.1:p.Ser4623Ala
XM_011543677.1:c.11251T>G	XP_011541979.1:p.Ser3751Ala
XM_011543678.1:c.13948T>G	XP_011541980.1:p.Ser4650Ala
NM_032119.4:c.13948T>G MANE Select	NP_115495.3:p.Ser4650Ala
XM_017009963.2:c.13969T>G	XP_016865452.1:p.Ser4657Ala
XM_017009964.2:c.13966T>G	XP_016865453.1:p.Ser4656Ala
XM_017009965.1:c.13966T>G	XP_016865454.1:p.Ser4656Ala
XM_017009966.2:c.13888T>G	XP_016865455.1:p.Ser4630Ala
XM_017009967.1:c.13873T>G	XP_016865456.1:p.Ser4625Ala
XM_017009968.2:c.13969T>G	XP_016865457.1:p.Ser4657Ala
XM_017009969.2:c.13969T>G	XP_016865458.1:p.Ser4657Ala
XM_017009970.2:c.13969T>G	XP_016865459.1:p.Ser4657Ala
XM_017009971.2:c.13969T>G	XP_016865460.1:p.Ser4657Ala
XM_017009972.1:c.7087T>G	XP_016865461.1:p.Ser2363Ala
XM_017009973.1:c.7066T>G	XP_016865462.1:p.Ser2356Ala
NR_003149.2:n.13964T>G