Canonical Allele Identifier: CA3342640

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91102330A>G , CM000667.2:g.91102330A>G	GRCh38
NC_000005.9:g.90398147A>G , CM000667.1:g.90398147A>G	GRCh37
NC_000005.8:g.90433903A>G	NCBI36
NG_007083.1:g.548531A>G
NG_007083.2:g.577987A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18422A>G MANE Select	NP_115495.3:p.Asn6141Ser
ENST00000405460.9:c.18422A>G MANE Select	ENSP00000384582.2:p.Asn6141Ser
NM_032119.3:c.18422A>G	NP_115495.3:p.Asn6141Ser
NR_003149.1:n.18435A>G
NR_003149.2:n.18438A>G
ENST00000405460.6:c.18422A>G	ENSP00000384582.2:p.Asn6141Ser
ENST00000425867.2:c.5405A>G	ENSP00000392618.2:p.Asn1802Ser
ENST00000425867.3:c.7376A>G	ENSP00000392618.3:p.Asn2459Ser
ENST00000638510.1:n.5689A>G
ENST00000638990.1:c.1634A>G
ENST00000639212.1:n.342A>G
ENST00000639530.1:n.290A>G
ENST00000639821.1:c.506A>G	ENSP00000492216.1:p.Asn169Ser
ENST00000640256.1:n.290A>G
ENST00000640407.1:c.4871A>G	ENSP00000491425.1:n.4871A>G
ENST00000640815.1:c.506A>G	ENSP00000491767.1:p.Asn169Ser
XM_011543675.1:c.18419A>G	XP_011541977.1:p.Asn6140Ser
XM_011543676.1:c.18341A>G	XP_011541978.1:p.Asn6114Ser
XM_011543677.1:c.15725A>G	XP_011541979.1:p.Asn5242Ser
XM_017009963.2:c.18443A>G	XP_016865452.1:p.Asn6148Ser
XM_017009964.2:c.18440A>G	XP_016865453.1:p.Asn6147Ser
XM_017009965.1:c.18440A>G	XP_016865454.1:p.Asn6147Ser
XM_017009966.2:c.18362A>G	XP_016865455.1:p.Asn6121Ser
XM_017009967.1:c.18347A>G	XP_016865456.1:p.Asn6116Ser
XM_017009968.2:c.18263A>G	XP_016865457.1:p.Asn6088Ser
XM_017009969.2:c.18443A>G	XP_016865458.1:p.Asn6148Ser
XM_017009972.1:c.11561A>G	XP_016865461.1:p.Asn3854Ser
XM_017009973.1:c.11540A>G	XP_016865462.1:p.Asn3847Ser