Canonical Allele Identifier: CA3341771

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90802853C>T , CM000667.2:g.90802853C>T	GRCh38
NC_000005.9:g.90098670C>T , CM000667.1:g.90098670C>T	GRCh37
NC_000005.8:g.90134426C>T	NCBI36
NG_007083.1:g.249054C>T
NG_007083.2:g.278510C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14632C>T MANE Select	NP_115495.3:p.Pro4878Ser
ENST00000405460.9:c.14632C>T MANE Select	ENSP00000384582.2:p.Pro4878Ser
NM_032119.3:c.14632C>T	NP_115495.3:p.Pro4878Ser
NR_003149.1:n.14645C>T
NR_003149.2:n.14648C>T
ENST00000405460.6:c.14632C>T	ENSP00000384582.2:p.Pro4878Ser
ENST00000425867.2:c.1615C>T	ENSP00000392618.2:p.Pro539Ser
ENST00000425867.3:c.3586C>T	ENSP00000392618.3:p.Pro1196Ser
ENST00000638510.1:n.1899C>T
ENST00000638585.1:n.398C>T
ENST00000639431.1:c.265+126644C>T	ENSP00000491057.1:n.265+126644C>T
ENST00000640407.1:c.1042C>T	ENSP00000491425.1:p.Pro348Ser
XM_011543675.1:c.14629C>T	XP_011541977.1:p.Pro4877Ser
XM_011543676.1:c.14551C>T	XP_011541978.1:p.Pro4851Ser
XM_011543677.1:c.11935C>T	XP_011541979.1:p.Pro3979Ser
XM_011543678.1:c.14632C>T	XP_011541980.1:p.Pro4878Ser
XM_017009963.2:c.14653C>T	XP_016865452.1:p.Pro4885Ser
XM_017009964.2:c.14650C>T	XP_016865453.1:p.Pro4884Ser
XM_017009965.1:c.14650C>T	XP_016865454.1:p.Pro4884Ser
XM_017009966.2:c.14572C>T	XP_016865455.1:p.Pro4858Ser
XM_017009967.1:c.14557C>T	XP_016865456.1:p.Pro4853Ser
XM_017009968.2:c.14653C>T	XP_016865457.1:p.Pro4885Ser
XM_017009969.2:c.14653C>T	XP_016865458.1:p.Pro4885Ser
XM_017009970.2:c.14653C>T	XP_016865459.1:p.Pro4885Ser
XM_017009971.2:c.14653C>T	XP_016865460.1:p.Pro4885Ser
XM_017009972.1:c.7771C>T	XP_016865461.1:p.Pro2591Ser
XM_017009973.1:c.7750C>T	XP_016865462.1:p.Pro2584Ser