Canonical Allele Identifier: CA360377407

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059161T>A (hg19) ; chr5:g.90763344T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763344T>A , CM000667.2:g.90763344T>A	GRCh38
NC_000005.9:g.90059161T>A , CM000667.1:g.90059161T>A	GRCh37
NC_000005.8:g.90094917T>A	NCBI36
NG_007083.1:g.209545T>A
NG_007083.2:g.239001T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12160T>A MANE Select	ENSP00000384582.2:p.Ser4054Thr
ENST00000425867.3:c.1114T>A	ENSP00000392618.3:p.Ser372Thr
ENST00000639431.1:c.265+87135T>A	ENSP00000491057.1:n.265+87135T>A
ENST00000640464.1:n.2579T>A
ENST00000640729.1:n.737T>A
ENST00000405460.6:c.12160T>A	ENSP00000384582.2:p.Ser4054Thr
NM_032119.3:c.12160T>A	NP_115495.3:p.Ser4054Thr
NR_003149.1:n.12173T>A
XM_011543675.1:c.12157T>A	XP_011541977.1:p.Ser4053Thr
XM_011543676.1:c.12079T>A	XP_011541978.1:p.Ser4027Thr
XM_011543677.1:c.9463T>A	XP_011541979.1:p.Ser3155Thr
XM_011543678.1:c.12160T>A	XP_011541980.1:p.Ser4054Thr
NM_032119.4:c.12160T>A MANE Select	NP_115495.3:p.Ser4054Thr
XM_017009963.2:c.12181T>A	XP_016865452.1:p.Ser4061Thr
XM_017009964.2:c.12178T>A	XP_016865453.1:p.Ser4060Thr
XM_017009965.1:c.12178T>A	XP_016865454.1:p.Ser4060Thr
XM_017009966.2:c.12100T>A	XP_016865455.1:p.Ser4034Thr
XM_017009967.1:c.12085T>A	XP_016865456.1:p.Ser4029Thr
XM_017009968.2:c.12181T>A	XP_016865457.1:p.Ser4061Thr
XM_017009969.2:c.12181T>A	XP_016865458.1:p.Ser4061Thr
XM_017009970.2:c.12181T>A	XP_016865459.1:p.Ser4061Thr
XM_017009971.2:c.12181T>A	XP_016865460.1:p.Ser4061Thr
XM_017009972.1:c.5299T>A	XP_016865461.1:p.Ser1767Thr
XM_017009973.1:c.5278T>A	XP_016865462.1:p.Ser1760Thr
NR_003149.2:n.12176T>A