Canonical Allele Identifier: CA3342104

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823501A>G , CM000667.2:g.90823501A>G	GRCh38
NC_000005.9:g.90119318A>G , CM000667.1:g.90119318A>G	GRCh37
NC_000005.8:g.90155074A>G	NCBI36
NG_007083.1:g.269702A>G
NG_007083.2:g.299158A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.16273A>G MANE Select	NP_115495.3:p.Asn5425Asp
ENST00000405460.9:c.16273A>G MANE Select	ENSP00000384582.2:p.Asn5425Asp
NM_032119.3:c.16273A>G	NP_115495.3:p.Asn5425Asp
NR_003149.1:n.16286A>G
NR_003149.2:n.16289A>G
ENST00000405460.6:c.16273A>G	ENSP00000384582.2:p.Asn5425Asp
ENST00000425867.2:c.3256A>G	ENSP00000392618.2:p.Asn1086Asp
ENST00000425867.3:c.5227A>G	ENSP00000392618.3:p.Asn1743Asp
ENST00000638510.1:n.3540A>G
ENST00000639431.1:c.265+147292A>G	ENSP00000491057.1:n.265+147292A>G
ENST00000640061.1:n.128+1319A>G
ENST00000640407.1:c.2683A>G	ENSP00000491425.1:p.Asn895Asp
XM_011543675.1:c.16270A>G	XP_011541977.1:p.Asn5424Asp
XM_011543676.1:c.16192A>G	XP_011541978.1:p.Asn5398Asp
XM_011543677.1:c.13576A>G	XP_011541979.1:p.Asn4526Asp
XM_017009963.2:c.16294A>G	XP_016865452.1:p.Asn5432Asp
XM_017009964.2:c.16291A>G	XP_016865453.1:p.Asn5431Asp
XM_017009965.1:c.16291A>G	XP_016865454.1:p.Asn5431Asp
XM_017009966.2:c.16213A>G	XP_016865455.1:p.Asn5405Asp
XM_017009967.1:c.16198A>G	XP_016865456.1:p.Asn5400Asp
XM_017009968.2:c.16114A>G	XP_016865457.1:p.Asn5372Asp
XM_017009969.2:c.16294A>G	XP_016865458.1:p.Asn5432Asp
XM_017009972.1:c.9412A>G	XP_016865461.1:p.Asn3138Asp
XM_017009973.1:c.9391A>G	XP_016865462.1:p.Asn3131Asp