Canonical Allele Identifier: CA360403188

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90021379T>A (hg19) ; chr5:g.90725562T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725562T>A , CM000667.2:g.90725562T>A	GRCh38
NC_000005.9:g.90021379T>A , CM000667.1:g.90021379T>A	GRCh37
NC_000005.8:g.90057135T>A	NCBI36
NG_007083.1:g.171763T>A
NG_007083.2:g.201219T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10067T>A MANE Select	ENSP00000384582.2:p.Ile3356Asn
ENST00000639431.1:c.265+49353T>A	ENSP00000491057.1:n.265+49353T>A
ENST00000640374.1:n.3211T>A
ENST00000640464.1:n.486T>A
ENST00000405460.6:c.10067T>A	ENSP00000384582.2:p.Ile3356Asn
ENST00000509621.1:c.2764T>A
NM_032119.3:c.10067T>A	NP_115495.3:p.Ile3356Asn
NR_003149.1:n.10080T>A
XM_011543675.1:c.10064T>A	XP_011541977.1:p.Ile3355Asn
XM_011543676.1:c.9986T>A	XP_011541978.1:p.Ile3329Asn
XM_011543677.1:c.7370T>A	XP_011541979.1:p.Ile2457Asn
XM_011543678.1:c.10067T>A	XP_011541980.1:p.Ile3356Asn
XM_011543679.1:c.10067T>A	XP_011541981.1:p.Ile3356Asn
XR_948560.1:n.272-9753A>T
NM_032119.4:c.10067T>A MANE Select	NP_115495.3:p.Ile3356Asn
XM_017009963.2:c.10088T>A	XP_016865452.1:p.Ile3363Asn
XM_017009964.2:c.10085T>A	XP_016865453.1:p.Ile3362Asn
XM_017009965.1:c.10085T>A	XP_016865454.1:p.Ile3362Asn
XM_017009966.2:c.10007T>A	XP_016865455.1:p.Ile3336Asn
XM_017009967.1:c.9992T>A	XP_016865456.1:p.Ile3331Asn
XM_017009968.2:c.10088T>A	XP_016865457.1:p.Ile3363Asn
XM_017009969.2:c.10088T>A	XP_016865458.1:p.Ile3363Asn
XM_017009970.2:c.10088T>A	XP_016865459.1:p.Ile3363Asn
XM_017009971.2:c.10088T>A	XP_016865460.1:p.Ile3363Asn
XM_017009972.1:c.3206T>A	XP_016865461.1:p.Ile1069Asn
XM_017009973.1:c.3185T>A	XP_016865462.1:p.Ile1062Asn
XM_017009974.2:c.10088T>A	XP_016865463.1:p.Ile3363Asn
XR_001742802.1:n.2523-9753A>T
NR_003149.2:n.10083T>A