Canonical Allele Identifier: CA360429314

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90985477A>G , CM000667.2:g.90985477A>G	GRCh38
NC_000005.9:g.90281294A>G , CM000667.1:g.90281294A>G	GRCh37
NC_000005.8:g.90317050A>G	NCBI36
NG_007083.1:g.431678A>G
NG_007083.2:g.461134A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18107A>G MANE Select	NP_115495.3:p.Tyr6036Cys
ENST00000405460.9:c.18107A>G MANE Select	ENSP00000384582.2:p.Tyr6036Cys
NM_032119.3:c.18107A>G	NP_115495.3:p.Tyr6036Cys
NR_003149.1:n.18120A>G
NR_003149.2:n.18123A>G
ENST00000405460.6:c.18107A>G	ENSP00000384582.2:p.Tyr6036Cys
ENST00000425867.2:c.5090A>G	ENSP00000392618.2:p.Tyr1697Cys
ENST00000425867.3:c.7061A>G	ENSP00000392618.3:p.Tyr2354Cys
ENST00000638510.1:n.5374A>G
ENST00000638990.1:c.1319A>G
ENST00000639431.1:c.399A>G	ENSP00000491057.1:n.399A>G
ENST00000639707.1:c.191A>G	ENSP00000492328.1:p.Tyr64Cys
ENST00000639821.1:c.191A>G	ENSP00000492216.1:p.Tyr64Cys
ENST00000640369.1:c.191A>G	ENSP00000491401.1:p.Tyr64Cys
ENST00000640407.1:c.4556A>G	ENSP00000491425.1:n.4556A>G
ENST00000640815.1:c.191A>G	ENSP00000491767.1:p.Tyr64Cys
XM_011543675.1:c.18104A>G	XP_011541977.1:p.Tyr6035Cys
XM_011543676.1:c.18026A>G	XP_011541978.1:p.Tyr6009Cys
XM_011543677.1:c.15410A>G	XP_011541979.1:p.Tyr5137Cys
XM_017009963.2:c.18128A>G	XP_016865452.1:p.Tyr6043Cys
XM_017009964.2:c.18125A>G	XP_016865453.1:p.Tyr6042Cys
XM_017009965.1:c.18125A>G	XP_016865454.1:p.Tyr6042Cys
XM_017009966.2:c.18047A>G	XP_016865455.1:p.Tyr6016Cys
XM_017009967.1:c.18032A>G	XP_016865456.1:p.Tyr6011Cys
XM_017009968.2:c.17948A>G	XP_016865457.1:p.Tyr5983Cys
XM_017009969.2:c.18128A>G	XP_016865458.1:p.Tyr6043Cys
XM_017009972.1:c.11246A>G	XP_016865461.1:p.Tyr3749Cys
XM_017009973.1:c.11225A>G	XP_016865462.1:p.Tyr3742Cys