Canonical Allele Identifier: CA360410698

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106817G>C (hg19) ; chr5:g.90811000G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811000G>C , CM000667.2:g.90811000G>C	GRCh38
NC_000005.9:g.90106817G>C , CM000667.1:g.90106817G>C	GRCh37
NC_000005.8:g.90142573G>C	NCBI36
NG_007083.1:g.257201G>C
NG_007083.2:g.286657G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15740G>C MANE Select	ENSP00000384582.2:p.Arg5247Thr
ENST00000425867.3:c.4694G>C	ENSP00000392618.3:p.Arg1565Thr
ENST00000638510.1:n.3007G>C
ENST00000639431.1:c.265+134791G>C	ENSP00000491057.1:n.265+134791G>C
ENST00000640407.1:c.2150G>C	ENSP00000491425.1:p.Arg717Thr
ENST00000405460.6:c.15740G>C	ENSP00000384582.2:p.Arg5247Thr
ENST00000425867.2:c.2723G>C	ENSP00000392618.2:p.Arg908Thr
NM_032119.3:c.15740G>C	NP_115495.3:p.Arg5247Thr
NR_003149.1:n.15753G>C
XM_011543675.1:c.15737G>C	XP_011541977.1:p.Arg5246Thr
XM_011543676.1:c.15659G>C	XP_011541978.1:p.Arg5220Thr
XM_011543677.1:c.13043G>C	XP_011541979.1:p.Arg4348Thr
NM_032119.4:c.15740G>C MANE Select	NP_115495.3:p.Arg5247Thr
XM_017009963.2:c.15761G>C	XP_016865452.1:p.Arg5254Thr
XM_017009964.2:c.15758G>C	XP_016865453.1:p.Arg5253Thr
XM_017009965.1:c.15758G>C	XP_016865454.1:p.Arg5253Thr
XM_017009966.2:c.15680G>C	XP_016865455.1:p.Arg5227Thr
XM_017009967.1:c.15665G>C	XP_016865456.1:p.Arg5222Thr
XM_017009968.2:c.15581G>C	XP_016865457.1:p.Arg5194Thr
XM_017009969.2:c.15761G>C	XP_016865458.1:p.Arg5254Thr
XM_017009972.1:c.8879G>C	XP_016865461.1:p.Arg2960Thr
XM_017009973.1:c.8858G>C	XP_016865462.1:p.Arg2953Thr
NR_003149.2:n.15756G>C