Canonical Allele Identifier: CA360409665

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106552A>T (hg19) ; chr5:g.90810735A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810735A>T , CM000667.2:g.90810735A>T	GRCh38
NC_000005.9:g.90106552A>T , CM000667.1:g.90106552A>T	GRCh37
NC_000005.8:g.90142308A>T	NCBI36
NG_007083.1:g.256936A>T
NG_007083.2:g.286392A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.15475A>T MANE Select	ENSP00000384582.2:p.Thr5159Ser
ENST00000425867.3:c.4429A>T	ENSP00000392618.3:p.Thr1477Ser
ENST00000638510.1:n.2742A>T
ENST00000639431.1:c.265+134526A>T	ENSP00000491057.1:n.265+134526A>T
ENST00000640407.1:c.1885A>T	ENSP00000491425.1:p.Thr629Ser
ENST00000405460.6:c.15475A>T	ENSP00000384582.2:p.Thr5159Ser
ENST00000425867.2:c.2458A>T	ENSP00000392618.2:p.Thr820Ser
NM_032119.3:c.15475A>T	NP_115495.3:p.Thr5159Ser
NR_003149.1:n.15488A>T
XM_011543675.1:c.15472A>T	XP_011541977.1:p.Thr5158Ser
XM_011543676.1:c.15394A>T	XP_011541978.1:p.Thr5132Ser
XM_011543677.1:c.12778A>T	XP_011541979.1:p.Thr4260Ser
NM_032119.4:c.15475A>T MANE Select	NP_115495.3:p.Thr5159Ser
XM_017009963.2:c.15496A>T	XP_016865452.1:p.Thr5166Ser
XM_017009964.2:c.15493A>T	XP_016865453.1:p.Thr5165Ser
XM_017009965.1:c.15493A>T	XP_016865454.1:p.Thr5165Ser
XM_017009966.2:c.15415A>T	XP_016865455.1:p.Thr5139Ser
XM_017009967.1:c.15400A>T	XP_016865456.1:p.Thr5134Ser
XM_017009968.2:c.15316A>T	XP_016865457.1:p.Thr5106Ser
XM_017009969.2:c.15496A>T	XP_016865458.1:p.Thr5166Ser
XM_017009971.2:c.*429A>T	XP_016865460.1:n.*429A>T
XM_017009972.1:c.8614A>T	XP_016865461.1:p.Thr2872Ser
XM_017009973.1:c.8593A>T	XP_016865462.1:p.Thr2865Ser
NR_003149.2:n.15491A>T