Canonical Allele Identifier: CA360403215

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90021391G>A (hg19) ; chr5:g.90725574G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725574G>A , CM000667.2:g.90725574G>A	GRCh38
NC_000005.9:g.90021391G>A , CM000667.1:g.90021391G>A	GRCh37
NC_000005.8:g.90057147G>A	NCBI36
NG_007083.1:g.171775G>A
NG_007083.2:g.201231G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10079G>A MANE Select	ENSP00000384582.2:p.Ser3360Asn
ENST00000639431.1:c.265+49365G>A	ENSP00000491057.1:n.265+49365G>A
ENST00000640374.1:n.3223G>A
ENST00000640464.1:n.498G>A
ENST00000405460.6:c.10079G>A	ENSP00000384582.2:p.Ser3360Asn
ENST00000509621.1:c.2776G>A
NM_032119.3:c.10079G>A	NP_115495.3:p.Ser3360Asn
NR_003149.1:n.10092G>A
XM_011543675.1:c.10076G>A	XP_011541977.1:p.Ser3359Asn
XM_011543676.1:c.9998G>A	XP_011541978.1:p.Ser3333Asn
XM_011543677.1:c.7382G>A	XP_011541979.1:p.Ser2461Asn
XM_011543678.1:c.10079G>A	XP_011541980.1:p.Ser3360Asn
XM_011543679.1:c.10079G>A	XP_011541981.1:p.Ser3360Asn
XR_948560.1:n.272-9765C>T
NM_032119.4:c.10079G>A MANE Select	NP_115495.3:p.Ser3360Asn
XM_017009963.2:c.10100G>A	XP_016865452.1:p.Ser3367Asn
XM_017009964.2:c.10097G>A	XP_016865453.1:p.Ser3366Asn
XM_017009965.1:c.10097G>A	XP_016865454.1:p.Ser3366Asn
XM_017009966.2:c.10019G>A	XP_016865455.1:p.Ser3340Asn
XM_017009967.1:c.10004G>A	XP_016865456.1:p.Ser3335Asn
XM_017009968.2:c.10100G>A	XP_016865457.1:p.Ser3367Asn
XM_017009969.2:c.10100G>A	XP_016865458.1:p.Ser3367Asn
XM_017009970.2:c.10100G>A	XP_016865459.1:p.Ser3367Asn
XM_017009971.2:c.10100G>A	XP_016865460.1:p.Ser3367Asn
XM_017009972.1:c.3218G>A	XP_016865461.1:p.Ser1073Asn
XM_017009973.1:c.3197G>A	XP_016865462.1:p.Ser1066Asn
XM_017009974.2:c.10100G>A	XP_016865463.1:p.Ser3367Asn
XR_001742802.1:n.2523-9765C>T
NR_003149.2:n.10095G>A