Canonical Allele Identifier: CA3342155

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90829011A>G , CM000667.2:g.90829011A>G	GRCh38
NC_000005.9:g.90124828A>G , CM000667.1:g.90124828A>G	GRCh37
NC_000005.8:g.90160584A>G	NCBI36
NG_007083.1:g.275212A>G
NG_007083.2:g.304668A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.16436A>G MANE Select	NP_115495.3:p.Asn5479Ser
ENST00000405460.9:c.16436A>G MANE Select	ENSP00000384582.2:p.Asn5479Ser
NM_032119.3:c.16436A>G	NP_115495.3:p.Asn5479Ser
NR_003149.1:n.16449A>G
NR_003149.2:n.16452A>G
ENST00000405460.6:c.16436A>G	ENSP00000384582.2:p.Asn5479Ser
ENST00000425867.2:c.3419A>G	ENSP00000392618.2:p.Asn1140Ser
ENST00000425867.3:c.5390A>G	ENSP00000392618.3:p.Asn1797Ser
ENST00000638510.1:n.3703A>G
ENST00000639431.1:c.265+152802A>G	ENSP00000491057.1:n.265+152802A>G
ENST00000640061.1:n.128+6829A>G
ENST00000640407.1:c.2885A>G	ENSP00000491425.1:n.2885A>G
XM_011543675.1:c.16433A>G	XP_011541977.1:p.Asn5478Ser
XM_011543676.1:c.16355A>G	XP_011541978.1:p.Asn5452Ser
XM_011543677.1:c.13739A>G	XP_011541979.1:p.Asn4580Ser
XM_017009963.2:c.16457A>G	XP_016865452.1:p.Asn5486Ser
XM_017009964.2:c.16454A>G	XP_016865453.1:p.Asn5485Ser
XM_017009965.1:c.16454A>G	XP_016865454.1:p.Asn5485Ser
XM_017009966.2:c.16376A>G	XP_016865455.1:p.Asn5459Ser
XM_017009967.1:c.16361A>G	XP_016865456.1:p.Asn5454Ser
XM_017009968.2:c.16277A>G	XP_016865457.1:p.Asn5426Ser
XM_017009969.2:c.16457A>G	XP_016865458.1:p.Asn5486Ser
XM_017009972.1:c.9575A>G	XP_016865461.1:p.Asn3192Ser
XM_017009973.1:c.9554A>G	XP_016865462.1:p.Asn3185Ser