Canonical Allele Identifier: CA360425512

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119276A>T (hg19) ; chr5:g.90823459A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823459A>T , CM000667.2:g.90823459A>T	GRCh38
NC_000005.9:g.90119276A>T , CM000667.1:g.90119276A>T	GRCh37
NC_000005.8:g.90155032A>T	NCBI36
NG_007083.1:g.269660A>T
NG_007083.2:g.299116A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16231A>T MANE Select	ENSP00000384582.2:p.Thr5411Ser
ENST00000425867.3:c.5185A>T	ENSP00000392618.3:p.Thr1729Ser
ENST00000638510.1:n.3498A>T
ENST00000639431.1:c.265+147250A>T	ENSP00000491057.1:n.265+147250A>T
ENST00000640061.1:n.128+1277A>T
ENST00000640407.1:c.2641A>T	ENSP00000491425.1:p.Thr881Ser
ENST00000405460.6:c.16231A>T	ENSP00000384582.2:p.Thr5411Ser
ENST00000425867.2:c.3214A>T	ENSP00000392618.2:p.Thr1072Ser
NM_032119.3:c.16231A>T	NP_115495.3:p.Thr5411Ser
NR_003149.1:n.16244A>T
XM_011543675.1:c.16228A>T	XP_011541977.1:p.Thr5410Ser
XM_011543676.1:c.16150A>T	XP_011541978.1:p.Thr5384Ser
XM_011543677.1:c.13534A>T	XP_011541979.1:p.Thr4512Ser
NM_032119.4:c.16231A>T MANE Select	NP_115495.3:p.Thr5411Ser
XM_017009963.2:c.16252A>T	XP_016865452.1:p.Thr5418Ser
XM_017009964.2:c.16249A>T	XP_016865453.1:p.Thr5417Ser
XM_017009965.1:c.16249A>T	XP_016865454.1:p.Thr5417Ser
XM_017009966.2:c.16171A>T	XP_016865455.1:p.Thr5391Ser
XM_017009967.1:c.16156A>T	XP_016865456.1:p.Thr5386Ser
XM_017009968.2:c.16072A>T	XP_016865457.1:p.Thr5358Ser
XM_017009969.2:c.16252A>T	XP_016865458.1:p.Thr5418Ser
XM_017009972.1:c.9370A>T	XP_016865461.1:p.Thr3124Ser
XM_017009973.1:c.9349A>T	XP_016865462.1:p.Thr3117Ser
NR_003149.2:n.16247A>T