Canonical Allele Identifier: CA3338602

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627592C>A , CM000667.2:g.90627592C>A	GRCh38
NC_000005.9:g.89923409C>A , CM000667.1:g.89923409C>A	GRCh37
NC_000005.8:g.89959165C>A	NCBI36
NG_007083.1:g.73793C>A
NG_007083.2:g.103249C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.1054C>A MANE Select	NP_115495.3:p.Pro352Thr
ENST00000405460.9:c.1054C>A MANE Select	ENSP00000384582.2:p.Pro352Thr
NM_032119.3:c.1054C>A	NP_115495.3:p.Pro352Thr
NR_003149.1:n.1150C>A
NR_003149.2:n.1153C>A
ENST00000405460.6:c.1054C>A	ENSP00000384582.2:p.Pro352Thr
ENST00000640083.1:n.759C>A
ENST00000640109.1:n.1150C>A
ENST00000640281.1:n.1113C>A
XM_011543675.1:c.1054C>A	XP_011541977.1:p.Pro352Thr
XM_011543676.1:c.1054C>A	XP_011541978.1:p.Pro352Thr
XM_011543678.1:c.1054C>A	XP_011541980.1:p.Pro352Thr
XM_011543679.1:c.1054C>A	XP_011541981.1:p.Pro352Thr
XM_017009963.2:c.1054C>A	XP_016865452.1:p.Pro352Thr
XM_017009964.2:c.1054C>A	XP_016865453.1:p.Pro352Thr
XM_017009965.1:c.1051C>A	XP_016865454.1:p.Pro351Thr
XM_017009966.2:c.1054C>A	XP_016865455.1:p.Pro352Thr
XM_017009967.1:c.958C>A	XP_016865456.1:p.Pro320Thr
XM_017009968.2:c.1054C>A	XP_016865457.1:p.Pro352Thr
XM_017009969.2:c.1054C>A	XP_016865458.1:p.Pro352Thr
XM_017009970.2:c.1054C>A	XP_016865459.1:p.Pro352Thr
XM_017009971.2:c.1054C>A	XP_016865460.1:p.Pro352Thr
XM_017009974.2:c.1054C>A	XP_016865463.1:p.Pro352Thr