Canonical Allele Identifier: CA360377742

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059188T>A (hg19) ; chr5:g.90763371T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763371T>A , CM000667.2:g.90763371T>A	GRCh38
NC_000005.9:g.90059188T>A , CM000667.1:g.90059188T>A	GRCh37
NC_000005.8:g.90094944T>A	NCBI36
NG_007083.1:g.209572T>A
NG_007083.2:g.239028T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12187T>A MANE Select	ENSP00000384582.2:p.Ser4063Thr
ENST00000425867.3:c.1141T>A	ENSP00000392618.3:p.Ser381Thr
ENST00000639431.1:c.265+87162T>A	ENSP00000491057.1:n.265+87162T>A
ENST00000640464.1:n.2606T>A
ENST00000640729.1:n.764T>A
ENST00000405460.6:c.12187T>A	ENSP00000384582.2:p.Ser4063Thr
NM_032119.3:c.12187T>A	NP_115495.3:p.Ser4063Thr
NR_003149.1:n.12200T>A
XM_011543675.1:c.12184T>A	XP_011541977.1:p.Ser4062Thr
XM_011543676.1:c.12106T>A	XP_011541978.1:p.Ser4036Thr
XM_011543677.1:c.9490T>A	XP_011541979.1:p.Ser3164Thr
XM_011543678.1:c.12187T>A	XP_011541980.1:p.Ser4063Thr
NM_032119.4:c.12187T>A MANE Select	NP_115495.3:p.Ser4063Thr
XM_017009963.2:c.12208T>A	XP_016865452.1:p.Ser4070Thr
XM_017009964.2:c.12205T>A	XP_016865453.1:p.Ser4069Thr
XM_017009965.1:c.12205T>A	XP_016865454.1:p.Ser4069Thr
XM_017009966.2:c.12127T>A	XP_016865455.1:p.Ser4043Thr
XM_017009967.1:c.12112T>A	XP_016865456.1:p.Ser4038Thr
XM_017009968.2:c.12208T>A	XP_016865457.1:p.Ser4070Thr
XM_017009969.2:c.12208T>A	XP_016865458.1:p.Ser4070Thr
XM_017009970.2:c.12208T>A	XP_016865459.1:p.Ser4070Thr
XM_017009971.2:c.12208T>A	XP_016865460.1:p.Ser4070Thr
XM_017009972.1:c.5326T>A	XP_016865461.1:p.Ser1776Thr
XM_017009973.1:c.5305T>A	XP_016865462.1:p.Ser1769Thr
NR_003149.2:n.12203T>A