Canonical Allele Identifier: CA360396354

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712395-T-A
• MyVariant Identifiers: chr5:g.90008212T>A (hg19) ; chr5:g.90712395T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712395T>A , CM000667.2:g.90712395T>A	GRCh38
NC_000005.9:g.90008212T>A , CM000667.1:g.90008212T>A	GRCh37
NC_000005.8:g.90043968T>A	NCBI36
NG_007083.1:g.158596T>A
NG_007083.2:g.188052T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9151T>A MANE Select	ENSP00000384582.2:p.Ser3051Thr
ENST00000639431.1:c.265+36186T>A	ENSP00000491057.1:n.265+36186T>A
ENST00000639473.1:n.4610T>A
ENST00000640012.1:c.2958T>A
ENST00000640374.1:n.2295T>A
ENST00000640779.1:c.3880T>A
ENST00000405460.6:c.9151T>A	ENSP00000384582.2:p.Ser3051Thr
ENST00000509621.1:c.1848T>A
NM_032119.3:c.9151T>A	NP_115495.3:p.Ser3051Thr
NR_003149.1:n.9164T>A
XM_011543675.1:c.9148T>A	XP_011541977.1:p.Ser3050Thr
XM_011543676.1:c.9070T>A	XP_011541978.1:p.Ser3024Thr
XM_011543677.1:c.6454T>A	XP_011541979.1:p.Ser2152Thr
XM_011543678.1:c.9151T>A	XP_011541980.1:p.Ser3051Thr
XM_011543679.1:c.9151T>A	XP_011541981.1:p.Ser3051Thr
XR_948560.1:n.451A>T
NM_032119.4:c.9151T>A MANE Select	NP_115495.3:p.Ser3051Thr
XM_017009963.2:c.9172T>A	XP_016865452.1:p.Ser3058Thr
XM_017009964.2:c.9169T>A	XP_016865453.1:p.Ser3057Thr
XM_017009965.1:c.9169T>A	XP_016865454.1:p.Ser3057Thr
XM_017009966.2:c.9091T>A	XP_016865455.1:p.Ser3031Thr
XM_017009967.1:c.9076T>A	XP_016865456.1:p.Ser3026Thr
XM_017009968.2:c.9172T>A	XP_016865457.1:p.Ser3058Thr
XM_017009969.2:c.9172T>A	XP_016865458.1:p.Ser3058Thr
XM_017009970.2:c.9172T>A	XP_016865459.1:p.Ser3058Thr
XM_017009971.2:c.9172T>A	XP_016865460.1:p.Ser3058Thr
XM_017009972.1:c.2290T>A	XP_016865461.1:p.Ser764Thr
XM_017009973.1:c.2269T>A	XP_016865462.1:p.Ser757Thr
XM_017009974.2:c.9172T>A	XP_016865463.1:p.Ser3058Thr
NR_003149.2:n.9167T>A