Canonical Allele Identifier: CA2840888068

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823571_90823572insGTTTGA , CM000667.2:g.90823571_90823572insGTTTGA	GRCh38
NC_000005.9:g.90119388_90119389insGTTTGA , CM000667.1:g.90119388_90119389insGTTTGA	GRCh37
NC_000005.8:g.90155144_90155145insGTTTGA	NCBI36
NG_007083.1:g.269772_269773insGTTTGA
NG_007083.2:g.299228_299229insGTTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16343_16344insGTTTGA MANE Select	ENSP00000384582.2:p.Ile5448delinsMetPheAsp
ENST00000425867.3:c.5297_5298insGTTTGA	ENSP00000392618.3:p.Ile1766delinsMetPheAsp
ENST00000638510.1:n.3610_3611insGTTTGA
ENST00000639431.1:c.265+147362_265+147363insGTTTGA	ENSP00000491057.1:n.265+147362_265+147363insGTTTGA
ENST00000640061.1:n.128+1389_128+1390insGTTTGA
ENST00000640407.1:c.2753_2754insGTTTGA	ENSP00000491425.1:p.Ile918delinsMetPheAsp
ENST00000405460.6:c.16343_16344insGTTTGA	ENSP00000384582.2:p.Ile5448delinsMetPheAsp
ENST00000425867.2:c.3326_3327insGTTTGA	ENSP00000392618.2:p.Ile1109delinsMetPheAsp
NM_032119.3:c.16343_16344insGTTTGA	NP_115495.3:p.Ile5448delinsMetPheAsp
NR_003149.1:n.16356_16357insGTTTGA
XM_011543675.1:c.16340_16341insGTTTGA	XP_011541977.1:p.Ile5447delinsMetPheAsp
XM_011543676.1:c.16262_16263insGTTTGA	XP_011541978.1:p.Ile5421delinsMetPheAsp
XM_011543677.1:c.13646_13647insGTTTGA	XP_011541979.1:p.Ile4549delinsMetPheAsp
NM_032119.4:c.16343_16344insGTTTGA MANE Select	NP_115495.3:p.Ile5448delinsMetPheAsp
XM_017009963.2:c.16364_16365insGTTTGA	XP_016865452.1:p.Ile5455delinsMetPheAsp
XM_017009964.2:c.16361_16362insGTTTGA	XP_016865453.1:p.Ile5454delinsMetPheAsp
XM_017009965.1:c.16361_16362insGTTTGA	XP_016865454.1:p.Ile5454delinsMetPheAsp
XM_017009966.2:c.16283_16284insGTTTGA	XP_016865455.1:p.Ile5428delinsMetPheAsp
XM_017009967.1:c.16268_16269insGTTTGA	XP_016865456.1:p.Ile5423delinsMetPheAsp
XM_017009968.2:c.16184_16185insGTTTGA	XP_016865457.1:p.Ile5395delinsMetPheAsp
XM_017009969.2:c.16364_16365insGTTTGA	XP_016865458.1:p.Ile5455delinsMetPheAsp
XM_017009972.1:c.9482_9483insGTTTGA	XP_016865461.1:p.Ile3161delinsMetPheAsp
XM_017009973.1:c.9461_9462insGTTTGA	XP_016865462.1:p.Ile3154delinsMetPheAsp
NR_003149.2:n.16359_16360insGTTTGA