Canonical Allele Identifier: CA360371602

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988542G>T (hg19) ; chr5:g.90692725G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692725G>T , CM000667.2:g.90692725G>T	GRCh38
NC_000005.9:g.89988542G>T , CM000667.1:g.89988542G>T	GRCh37
NC_000005.8:g.90024298G>T	NCBI36
NG_007083.1:g.138926G>T
NG_007083.2:g.168382G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7072G>T MANE Select	ENSP00000384582.2:p.Val2358Phe
ENST00000639431.1:c.265+16516G>T	ENSP00000491057.1:n.265+16516G>T
ENST00000639473.1:n.2531G>T
ENST00000640012.1:c.879G>T
ENST00000640374.1:n.216G>T
ENST00000640403.1:c.4363G>T	ENSP00000492531.1:p.Val1455Phe
ENST00000640779.1:c.1801G>T
ENST00000405460.6:c.7072G>T	ENSP00000384582.2:p.Val2358Phe
NM_032119.3:c.7072G>T	NP_115495.3:p.Val2358Phe
NR_003149.1:n.7085G>T
XM_011543675.1:c.7069G>T	XP_011541977.1:p.Val2357Phe
XM_011543676.1:c.6991G>T	XP_011541978.1:p.Val2331Phe
XM_011543677.1:c.4375G>T	XP_011541979.1:p.Val1459Phe
XM_011543678.1:c.7072G>T	XP_011541980.1:p.Val2358Phe
XM_011543679.1:c.7072G>T	XP_011541981.1:p.Val2358Phe
NM_032119.4:c.7072G>T MANE Select	NP_115495.3:p.Val2358Phe
XM_017009963.2:c.7072G>T	XP_016865452.1:p.Val2358Phe
XM_017009964.2:c.7069G>T	XP_016865453.1:p.Val2357Phe
XM_017009965.1:c.7069G>T	XP_016865454.1:p.Val2357Phe
XM_017009966.2:c.6991G>T	XP_016865455.1:p.Val2331Phe
XM_017009967.1:c.6976G>T	XP_016865456.1:p.Val2326Phe
XM_017009968.2:c.7072G>T	XP_016865457.1:p.Val2358Phe
XM_017009969.2:c.7072G>T	XP_016865458.1:p.Val2358Phe
XM_017009970.2:c.7072G>T	XP_016865459.1:p.Val2358Phe
XM_017009971.2:c.7072G>T	XP_016865460.1:p.Val2358Phe
XM_017009972.1:c.190G>T	XP_016865461.1:p.Val64Phe
XM_017009973.1:c.190G>T	XP_016865462.1:p.Val64Phe
XM_017009974.2:c.7072G>T	XP_016865463.1:p.Val2358Phe
NR_003149.2:n.7088G>T