Canonical Allele Identifier: CA3342539

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90985377G>C , CM000667.2:g.90985377G>C	GRCh38
NC_000005.9:g.90281194G>C , CM000667.1:g.90281194G>C	GRCh37
NC_000005.8:g.90316950G>C	NCBI36
NG_007083.1:g.431578G>C
NG_007083.2:g.461034G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18007G>C MANE Select	NP_115495.3:p.Asp6003His
ENST00000405460.9:c.18007G>C MANE Select	ENSP00000384582.2:p.Asp6003His
NM_032119.3:c.18007G>C	NP_115495.3:p.Asp6003His
NR_003149.1:n.18020G>C
NR_003149.2:n.18023G>C
ENST00000405460.6:c.18007G>C	ENSP00000384582.2:p.Asp6003His
ENST00000425867.2:c.4990G>C	ENSP00000392618.2:p.Asp1664His
ENST00000425867.3:c.6961G>C	ENSP00000392618.3:p.Asp2321His
ENST00000638510.1:n.5274G>C
ENST00000638990.1:c.1219G>C
ENST00000639431.1:c.299G>C	ENSP00000491057.1:p.Ter100Ser
ENST00000639707.1:c.91G>C	ENSP00000492328.1:p.Asp31His
ENST00000639821.1:c.91G>C	ENSP00000492216.1:p.Asp31His
ENST00000640369.1:c.91G>C	ENSP00000491401.1:p.Asp31His
ENST00000640407.1:c.4456G>C	ENSP00000491425.1:n.4456G>C
ENST00000640815.1:c.91G>C	ENSP00000491767.1:p.Asp31His
XM_011543675.1:c.18004G>C	XP_011541977.1:p.Asp6002His
XM_011543676.1:c.17926G>C	XP_011541978.1:p.Asp5976His
XM_011543677.1:c.15310G>C	XP_011541979.1:p.Asp5104His
XM_017009963.2:c.18028G>C	XP_016865452.1:p.Asp6010His
XM_017009964.2:c.18025G>C	XP_016865453.1:p.Asp6009His
XM_017009965.1:c.18025G>C	XP_016865454.1:p.Asp6009His
XM_017009966.2:c.17947G>C	XP_016865455.1:p.Asp5983His
XM_017009967.1:c.17932G>C	XP_016865456.1:p.Asp5978His
XM_017009968.2:c.17848G>C	XP_016865457.1:p.Asp5950His
XM_017009969.2:c.18028G>C	XP_016865458.1:p.Asp6010His
XM_017009972.1:c.11146G>C	XP_016865461.1:p.Asp3716His
XM_017009973.1:c.11125G>C	XP_016865462.1:p.Asp3709His