Canonical Allele Identifier: CA3342111

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823536C>T , CM000667.2:g.90823536C>T	GRCh38
NC_000005.9:g.90119353C>T , CM000667.1:g.90119353C>T	GRCh37
NC_000005.8:g.90155109C>T	NCBI36
NG_007083.1:g.269737C>T
NG_007083.2:g.299193C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.16308C>T MANE Select	NP_115495.3:p.Thr5436=
ENST00000405460.9:c.16308C>T MANE Select	ENSP00000384582.2:p.Thr5436=
NM_032119.3:c.16308C>T	NP_115495.3:p.Thr5436=
NR_003149.1:n.16321C>T
NR_003149.2:n.16324C>T
ENST00000405460.6:c.16308C>T	ENSP00000384582.2:p.Thr5436=
ENST00000425867.2:c.3291C>T	ENSP00000392618.2:p.Thr1097=
ENST00000425867.3:c.5262C>T	ENSP00000392618.3:p.Thr1754=
ENST00000638510.1:n.3575C>T
ENST00000639431.1:c.265+147327C>T	ENSP00000491057.1:n.265+147327C>T
ENST00000640061.1:n.128+1354C>T
ENST00000640407.1:c.2718C>T	ENSP00000491425.1:p.Thr906=
XM_011543675.1:c.16305C>T	XP_011541977.1:p.Thr5435=
XM_011543676.1:c.16227C>T	XP_011541978.1:p.Thr5409=
XM_011543677.1:c.13611C>T	XP_011541979.1:p.Thr4537=
XM_017009963.2:c.16329C>T	XP_016865452.1:p.Thr5443=
XM_017009964.2:c.16326C>T	XP_016865453.1:p.Thr5442=
XM_017009965.1:c.16326C>T	XP_016865454.1:p.Thr5442=
XM_017009966.2:c.16248C>T	XP_016865455.1:p.Thr5416=
XM_017009967.1:c.16233C>T	XP_016865456.1:p.Thr5411=
XM_017009968.2:c.16149C>T	XP_016865457.1:p.Thr5383=
XM_017009969.2:c.16329C>T	XP_016865458.1:p.Thr5443=
XM_017009972.1:c.9447C>T	XP_016865461.1:p.Thr3149=
XM_017009973.1:c.9426C>T	XP_016865462.1:p.Thr3142=