Canonical Allele Identifier: CA360401224

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086916A>T (hg19) ; chr5:g.90791099A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791099A>T , CM000667.2:g.90791099A>T	GRCh38
NC_000005.9:g.90086916A>T , CM000667.1:g.90086916A>T	GRCh37
NC_000005.8:g.90122672A>T	NCBI36
NG_007083.1:g.237300A>T
NG_007083.2:g.266756A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14270A>T MANE Select	ENSP00000384582.2:p.Asn4757Ile
ENST00000425867.3:c.3224A>T	ENSP00000392618.3:p.Asn1075Ile
ENST00000638510.1:n.1537A>T
ENST00000638585.1:n.36A>T
ENST00000638975.1:c.899A>T	ENSP00000492630.1:p.Asn300Ile
ENST00000639431.1:c.265+114890A>T	ENSP00000491057.1:n.265+114890A>T
ENST00000640407.1:c.680A>T	ENSP00000491425.1:p.Asn227Ile
ENST00000405460.6:c.14270A>T	ENSP00000384582.2:p.Asn4757Ile
ENST00000425867.2:c.1253A>T	ENSP00000392618.2:p.Asn418Ile
NM_032119.3:c.14270A>T	NP_115495.3:p.Asn4757Ile
NR_003149.1:n.14283A>T
XM_011543675.1:c.14267A>T	XP_011541977.1:p.Asn4756Ile
XM_011543676.1:c.14189A>T	XP_011541978.1:p.Asn4730Ile
XM_011543677.1:c.11573A>T	XP_011541979.1:p.Asn3858Ile
XM_011543678.1:c.14270A>T	XP_011541980.1:p.Asn4757Ile
NM_032119.4:c.14270A>T MANE Select	NP_115495.3:p.Asn4757Ile
XM_017009963.2:c.14291A>T	XP_016865452.1:p.Asn4764Ile
XM_017009964.2:c.14288A>T	XP_016865453.1:p.Asn4763Ile
XM_017009965.1:c.14288A>T	XP_016865454.1:p.Asn4763Ile
XM_017009966.2:c.14210A>T	XP_016865455.1:p.Asn4737Ile
XM_017009967.1:c.14195A>T	XP_016865456.1:p.Asn4732Ile
XM_017009968.2:c.14291A>T	XP_016865457.1:p.Asn4764Ile
XM_017009969.2:c.14291A>T	XP_016865458.1:p.Asn4764Ile
XM_017009970.2:c.14291A>T	XP_016865459.1:p.Asn4764Ile
XM_017009971.2:c.14291A>T	XP_016865460.1:p.Asn4764Ile
XM_017009972.1:c.7409A>T	XP_016865461.1:p.Asn2470Ile
XM_017009973.1:c.7388A>T	XP_016865462.1:p.Asn2463Ile
NR_003149.2:n.14286A>T