Canonical Allele Identifier: CA360409581

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041579T>G (hg19) ; chr5:g.90745762T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745762T>G , CM000667.2:g.90745762T>G	GRCh38
NC_000005.9:g.90041579T>G , CM000667.1:g.90041579T>G	GRCh37
NC_000005.8:g.90077335T>G	NCBI36
NG_007083.1:g.191963T>G
NG_007083.2:g.221419T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10941T>G MANE Select	ENSP00000384582.2:p.Asn3647Lys
ENST00000425867.3:c.72T>G	ENSP00000392618.3:p.Asn24Lys
ENST00000639431.1:c.265+69553T>G	ENSP00000491057.1:n.265+69553T>G
ENST00000640374.1:n.4085T>G
ENST00000640464.1:n.1360T>G
ENST00000405460.6:c.10941T>G	ENSP00000384582.2:p.Asn3647Lys
ENST00000509621.1:c.3638T>G
NM_032119.3:c.10941T>G	NP_115495.3:p.Asn3647Lys
NR_003149.1:n.10954T>G
XM_011543675.1:c.10938T>G	XP_011541977.1:p.Asn3646Lys
XM_011543676.1:c.10860T>G	XP_011541978.1:p.Asn3620Lys
XM_011543677.1:c.8244T>G	XP_011541979.1:p.Asn2748Lys
XM_011543678.1:c.10941T>G	XP_011541980.1:p.Asn3647Lys
NM_032119.4:c.10941T>G MANE Select	NP_115495.3:p.Asn3647Lys
XM_017009963.2:c.10962T>G	XP_016865452.1:p.Asn3654Lys
XM_017009964.2:c.10959T>G	XP_016865453.1:p.Asn3653Lys
XM_017009965.1:c.10959T>G	XP_016865454.1:p.Asn3653Lys
XM_017009966.2:c.10881T>G	XP_016865455.1:p.Asn3627Lys
XM_017009967.1:c.10866T>G	XP_016865456.1:p.Asn3622Lys
XM_017009968.2:c.10962T>G	XP_016865457.1:p.Asn3654Lys
XM_017009969.2:c.10962T>G	XP_016865458.1:p.Asn3654Lys
XM_017009970.2:c.10962T>G	XP_016865459.1:p.Asn3654Lys
XM_017009971.2:c.10962T>G	XP_016865460.1:p.Asn3654Lys
XM_017009972.1:c.4080T>G	XP_016865461.1:p.Asn1360Lys
XM_017009973.1:c.4059T>G	XP_016865462.1:p.Asn1353Lys
NR_003149.2:n.10957T>G