Canonical Allele Identifier: CA360399435

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720081C>T , CM000667.2:g.90720081C>T	GRCh38
NC_000005.9:g.90015898C>T , CM000667.1:g.90015898C>T	GRCh37
NC_000005.8:g.90051654C>T	NCBI36
NG_007083.1:g.166282C>T
NG_007083.2:g.195738C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9481C>T MANE Select	NP_115495.3:p.Pro3161Ser
ENST00000405460.9:c.9481C>T MANE Select	ENSP00000384582.2:p.Pro3161Ser
NM_032119.3:c.9481C>T	NP_115495.3:p.Pro3161Ser
NR_003149.1:n.9494C>T
NR_003149.2:n.9497C>T
ENST00000405460.6:c.9481C>T	ENSP00000384582.2:p.Pro3161Ser
ENST00000509621.1:c.2178C>T
ENST00000639431.1:c.265+43872C>T	ENSP00000491057.1:n.265+43872C>T
ENST00000640374.1:n.2625C>T
ENST00000640779.1:c.4210C>T
XM_011543675.1:c.9478C>T	XP_011541977.1:p.Pro3160Ser
XM_011543676.1:c.9400C>T	XP_011541978.1:p.Pro3134Ser
XM_011543677.1:c.6784C>T	XP_011541979.1:p.Pro2262Ser
XM_011543678.1:c.9481C>T	XP_011541980.1:p.Pro3161Ser
XM_011543679.1:c.9481C>T	XP_011541981.1:p.Pro3161Ser
XM_017009963.2:c.9502C>T	XP_016865452.1:p.Pro3168Ser
XM_017009964.2:c.9499C>T	XP_016865453.1:p.Pro3167Ser
XM_017009965.1:c.9499C>T	XP_016865454.1:p.Pro3167Ser
XM_017009966.2:c.9421C>T	XP_016865455.1:p.Pro3141Ser
XM_017009967.1:c.9406C>T	XP_016865456.1:p.Pro3136Ser
XM_017009968.2:c.9502C>T	XP_016865457.1:p.Pro3168Ser
XM_017009969.2:c.9502C>T	XP_016865458.1:p.Pro3168Ser
XM_017009970.2:c.9502C>T	XP_016865459.1:p.Pro3168Ser
XM_017009971.2:c.9502C>T	XP_016865460.1:p.Pro3168Ser
XM_017009972.1:c.2620C>T	XP_016865461.1:p.Pro874Ser
XM_017009973.1:c.2599C>T	XP_016865462.1:p.Pro867Ser
XM_017009974.2:c.9502C>T	XP_016865463.1:p.Pro3168Ser
XR_001742802.1:n.2523-4272G>A
XR_948560.1:n.272-4272G>A