Canonical Allele Identifier: CA3342506

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90965472G>A , CM000667.2:g.90965472G>A	GRCh38
NC_000005.9:g.90261289G>A , CM000667.1:g.90261289G>A	GRCh37
NC_000005.8:g.90297045G>A	NCBI36
NG_007083.1:g.411673G>A
NG_007083.2:g.441129G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17914G>A MANE Select	NP_115495.3:p.Ala5972Thr
ENST00000405460.9:c.17914G>A MANE Select	ENSP00000384582.2:p.Ala5972Thr
NM_032119.3:c.17914G>A	NP_115495.3:p.Ala5972Thr
NR_003149.1:n.17927G>A
NR_003149.2:n.17930G>A
ENST00000405460.6:c.17914G>A	ENSP00000384582.2:p.Ala5972Thr
ENST00000425867.2:c.4897G>A	ENSP00000392618.2:p.Ala1633Thr
ENST00000425867.3:c.6868G>A	ENSP00000392618.3:p.Ala2290Thr
ENST00000638510.1:n.5181G>A
ENST00000638990.1:c.1126G>A
ENST00000639431.1:c.266-19872G>A	ENSP00000491057.1:n.266-19872G>A
ENST00000639707.1:c.-3G>A	ENSP00000492328.1:n.-3G>A
ENST00000639821.1:c.-3G>A	ENSP00000492216.1:n.-3G>A
ENST00000640369.1:c.-3G>A	ENSP00000491401.1:n.-3G>A
ENST00000640407.1:c.4363G>A	ENSP00000491425.1:n.4363G>A
ENST00000640815.1:c.-3G>A	ENSP00000491767.1:n.-3G>A
XM_011543675.1:c.17911G>A	XP_011541977.1:p.Ala5971Thr
XM_011543676.1:c.17833G>A	XP_011541978.1:p.Ala5945Thr
XM_011543677.1:c.15217G>A	XP_011541979.1:p.Ala5073Thr
XM_017009963.2:c.17935G>A	XP_016865452.1:p.Ala5979Thr
XM_017009964.2:c.17932G>A	XP_016865453.1:p.Ala5978Thr
XM_017009965.1:c.17932G>A	XP_016865454.1:p.Ala5978Thr
XM_017009966.2:c.17854G>A	XP_016865455.1:p.Ala5952Thr
XM_017009967.1:c.17839G>A	XP_016865456.1:p.Ala5947Thr
XM_017009968.2:c.17755G>A	XP_016865457.1:p.Ala5919Thr
XM_017009969.2:c.17935G>A	XP_016865458.1:p.Ala5979Thr
XM_017009972.1:c.11053G>A	XP_016865461.1:p.Ala3685Thr
XM_017009973.1:c.11032G>A	XP_016865462.1:p.Ala3678Thr