Canonical Allele Identifier: CA3341931

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810757C>T , CM000667.2:g.90810757C>T	GRCh38
NC_000005.9:g.90106574C>T , CM000667.1:g.90106574C>T	GRCh37
NC_000005.8:g.90142330C>T	NCBI36
NG_007083.1:g.256958C>T
NG_007083.2:g.286414C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15497C>T MANE Select	NP_115495.3:p.Thr5166Met
ENST00000405460.9:c.15497C>T MANE Select	ENSP00000384582.2:p.Thr5166Met
NM_032119.3:c.15497C>T	NP_115495.3:p.Thr5166Met
NR_003149.1:n.15510C>T
NR_003149.2:n.15513C>T
ENST00000405460.6:c.15497C>T	ENSP00000384582.2:p.Thr5166Met
ENST00000425867.2:c.2480C>T	ENSP00000392618.2:p.Thr827Met
ENST00000425867.3:c.4451C>T	ENSP00000392618.3:p.Thr1484Met
ENST00000638510.1:n.2764C>T
ENST00000639431.1:c.265+134548C>T	ENSP00000491057.1:n.265+134548C>T
ENST00000640407.1:c.1907C>T	ENSP00000491425.1:p.Thr636Met
XM_011543675.1:c.15494C>T	XP_011541977.1:p.Thr5165Met
XM_011543676.1:c.15416C>T	XP_011541978.1:p.Thr5139Met
XM_011543677.1:c.12800C>T	XP_011541979.1:p.Thr4267Met
XM_017009963.2:c.15518C>T	XP_016865452.1:p.Thr5173Met
XM_017009964.2:c.15515C>T	XP_016865453.1:p.Thr5172Met
XM_017009965.1:c.15515C>T	XP_016865454.1:p.Thr5172Met
XM_017009966.2:c.15437C>T	XP_016865455.1:p.Thr5146Met
XM_017009967.1:c.15422C>T	XP_016865456.1:p.Thr5141Met
XM_017009968.2:c.15338C>T	XP_016865457.1:p.Thr5113Met
XM_017009969.2:c.15518C>T	XP_016865458.1:p.Thr5173Met
XM_017009971.2:c.*451C>T	XP_016865460.1:n.*451C>T
XM_017009972.1:c.8636C>T	XP_016865461.1:p.Thr2879Met
XM_017009973.1:c.8615C>T	XP_016865462.1:p.Thr2872Met