Canonical Allele Identifier: CA3342591

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91072503C>T , CM000667.2:g.91072503C>T	GRCh38
NC_000005.9:g.90368320C>T , CM000667.1:g.90368320C>T	GRCh37
NC_000005.8:g.90404076C>T	NCBI36
NG_007083.1:g.518704C>T
NG_007083.2:g.548160C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18209C>T MANE Select	NP_115495.3:p.Thr6070Met
ENST00000405460.9:c.18209C>T MANE Select	ENSP00000384582.2:p.Thr6070Met
NM_032119.3:c.18209C>T	NP_115495.3:p.Thr6070Met
NR_003149.1:n.18222C>T
NR_003149.2:n.18225C>T
ENST00000405460.6:c.18209C>T	ENSP00000384582.2:p.Thr6070Met
ENST00000425867.2:c.5192C>T	ENSP00000392618.2:p.Thr1731Met
ENST00000425867.3:c.7163C>T	ENSP00000392618.3:p.Thr2388Met
ENST00000638510.1:n.5476C>T
ENST00000638990.1:c.1421C>T
ENST00000639431.1:c.501C>T	ENSP00000491057.1:n.501C>T
ENST00000639707.1:c.293C>T	ENSP00000492328.1:p.Thr98Met
ENST00000639821.1:c.293C>T	ENSP00000492216.1:p.Thr98Met
ENST00000640369.1:c.293C>T	ENSP00000491401.1:p.Thr98Met
ENST00000640407.1:c.4658C>T	ENSP00000491425.1:n.4658C>T
ENST00000640815.1:c.293C>T	ENSP00000491767.1:p.Thr98Met
XM_011543675.1:c.18206C>T	XP_011541977.1:p.Thr6069Met
XM_011543676.1:c.18128C>T	XP_011541978.1:p.Thr6043Met
XM_011543677.1:c.15512C>T	XP_011541979.1:p.Thr5171Met
XM_017009963.2:c.18230C>T	XP_016865452.1:p.Thr6077Met
XM_017009964.2:c.18227C>T	XP_016865453.1:p.Thr6076Met
XM_017009965.1:c.18227C>T	XP_016865454.1:p.Thr6076Met
XM_017009966.2:c.18149C>T	XP_016865455.1:p.Thr6050Met
XM_017009967.1:c.18134C>T	XP_016865456.1:p.Thr6045Met
XM_017009968.2:c.18050C>T	XP_016865457.1:p.Thr6017Met
XM_017009969.2:c.18230C>T	XP_016865458.1:p.Thr6077Met
XM_017009972.1:c.11348C>T	XP_016865461.1:p.Thr3783Met
XM_017009973.1:c.11327C>T	XP_016865462.1:p.Thr3776Met