Canonical Allele Identifier: CA445436547

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119299G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823482G>T , CM000667.2:g.90823482G>T	GRCh38
NC_000005.9:g.90119299G>T , CM000667.1:g.90119299G>T	GRCh37
NC_000005.8:g.90155055G>T	NCBI36
NG_007083.1:g.269683G>T
NG_007083.2:g.299139G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16254G>T MANE Select	ENSP00000384582.2:p.Val5418=
ENST00000425867.3:c.5208G>T	ENSP00000392618.3:p.Val1736=
ENST00000638510.1:n.3521G>T
ENST00000639431.1:c.265+147273G>T	ENSP00000491057.1:n.265+147273G>T
ENST00000640061.1:n.128+1300G>T
ENST00000640407.1:c.2664G>T	ENSP00000491425.1:p.Val888=
ENST00000405460.6:c.16254G>T	ENSP00000384582.2:p.Val5418=
ENST00000425867.2:c.3237G>T	ENSP00000392618.2:p.Val1079=
NM_032119.3:c.16254G>T	NP_115495.3:p.Val5418=
NR_003149.1:n.16267G>T
XM_011543675.1:c.16251G>T	XP_011541977.1:p.Val5417=
XM_011543676.1:c.16173G>T	XP_011541978.1:p.Val5391=
XM_011543677.1:c.13557G>T	XP_011541979.1:p.Val4519=
NM_032119.4:c.16254G>T MANE Select	NP_115495.3:p.Val5418=
XM_017009963.2:c.16275G>T	XP_016865452.1:p.Val5425=
XM_017009964.2:c.16272G>T	XP_016865453.1:p.Val5424=
XM_017009965.1:c.16272G>T	XP_016865454.1:p.Val5424=
XM_017009966.2:c.16194G>T	XP_016865455.1:p.Val5398=
XM_017009967.1:c.16179G>T	XP_016865456.1:p.Val5393=
XM_017009968.2:c.16095G>T	XP_016865457.1:p.Val5365=
XM_017009969.2:c.16275G>T	XP_016865458.1:p.Val5425=
XM_017009972.1:c.9393G>T	XP_016865461.1:p.Val3131=
XM_017009973.1:c.9372G>T	XP_016865462.1:p.Val3124=
NR_003149.2:n.16270G>T