Canonical Allele Identifier: CA360425458

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119250A>T (hg19) ; chr5:g.90823433A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823433A>T , CM000667.2:g.90823433A>T	GRCh38
NC_000005.9:g.90119250A>T , CM000667.1:g.90119250A>T	GRCh37
NC_000005.8:g.90155006A>T	NCBI36
NG_007083.1:g.269634A>T
NG_007083.2:g.299090A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16205A>T MANE Select	ENSP00000384582.2:p.Glu5402Val
ENST00000425867.3:c.5159A>T	ENSP00000392618.3:p.Glu1720Val
ENST00000638510.1:n.3472A>T
ENST00000639431.1:c.265+147224A>T	ENSP00000491057.1:n.265+147224A>T
ENST00000640061.1:n.128+1251A>T
ENST00000640407.1:c.2615A>T	ENSP00000491425.1:p.Glu872Val
ENST00000405460.6:c.16205A>T	ENSP00000384582.2:p.Glu5402Val
ENST00000425867.2:c.3188A>T	ENSP00000392618.2:p.Glu1063Val
NM_032119.3:c.16205A>T	NP_115495.3:p.Glu5402Val
NR_003149.1:n.16218A>T
XM_011543675.1:c.16202A>T	XP_011541977.1:p.Glu5401Val
XM_011543676.1:c.16124A>T	XP_011541978.1:p.Glu5375Val
XM_011543677.1:c.13508A>T	XP_011541979.1:p.Glu4503Val
NM_032119.4:c.16205A>T MANE Select	NP_115495.3:p.Glu5402Val
XM_017009963.2:c.16226A>T	XP_016865452.1:p.Glu5409Val
XM_017009964.2:c.16223A>T	XP_016865453.1:p.Glu5408Val
XM_017009965.1:c.16223A>T	XP_016865454.1:p.Glu5408Val
XM_017009966.2:c.16145A>T	XP_016865455.1:p.Glu5382Val
XM_017009967.1:c.16130A>T	XP_016865456.1:p.Glu5377Val
XM_017009968.2:c.16046A>T	XP_016865457.1:p.Glu5349Val
XM_017009969.2:c.16226A>T	XP_016865458.1:p.Glu5409Val
XM_017009972.1:c.9344A>T	XP_016865461.1:p.Glu3115Val
XM_017009973.1:c.9323A>T	XP_016865462.1:p.Glu3108Val
NR_003149.2:n.16221A>T