Canonical Allele Identifier: CA360408894

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041440G>C (hg19) ; chr5:g.90745623G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745623G>C , CM000667.2:g.90745623G>C	GRCh38
NC_000005.9:g.90041440G>C , CM000667.1:g.90041440G>C	GRCh37
NC_000005.8:g.90077196G>C	NCBI36
NG_007083.1:g.191824G>C
NG_007083.2:g.221280G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10802G>C MANE Select	ENSP00000384582.2:p.Arg3601Thr
ENST00000639431.1:c.265+69414G>C	ENSP00000491057.1:n.265+69414G>C
ENST00000640374.1:n.3946G>C
ENST00000640464.1:n.1221G>C
ENST00000405460.6:c.10802G>C	ENSP00000384582.2:p.Arg3601Thr
ENST00000509621.1:c.3499G>C
NM_032119.3:c.10802G>C	NP_115495.3:p.Arg3601Thr
NR_003149.1:n.10815G>C
XM_011543675.1:c.10799G>C	XP_011541977.1:p.Arg3600Thr
XM_011543676.1:c.10721G>C	XP_011541978.1:p.Arg3574Thr
XM_011543677.1:c.8105G>C	XP_011541979.1:p.Arg2702Thr
XM_011543678.1:c.10802G>C	XP_011541980.1:p.Arg3601Thr
XM_011543679.1:c.*24G>C	XP_011541981.1:n.*24G>C
NM_032119.4:c.10802G>C MANE Select	NP_115495.3:p.Arg3601Thr
XM_017009963.2:c.10823G>C	XP_016865452.1:p.Arg3608Thr
XM_017009964.2:c.10820G>C	XP_016865453.1:p.Arg3607Thr
XM_017009965.1:c.10820G>C	XP_016865454.1:p.Arg3607Thr
XM_017009966.2:c.10742G>C	XP_016865455.1:p.Arg3581Thr
XM_017009967.1:c.10727G>C	XP_016865456.1:p.Arg3576Thr
XM_017009968.2:c.10823G>C	XP_016865457.1:p.Arg3608Thr
XM_017009969.2:c.10823G>C	XP_016865458.1:p.Arg3608Thr
XM_017009970.2:c.10823G>C	XP_016865459.1:p.Arg3608Thr
XM_017009971.2:c.10823G>C	XP_016865460.1:p.Arg3608Thr
XM_017009972.1:c.3941G>C	XP_016865461.1:p.Arg1314Thr
XM_017009973.1:c.3920G>C	XP_016865462.1:p.Arg1307Thr
XM_017009974.2:c.*24G>C	XP_016865463.1:n.*24G>C
NR_003149.2:n.10818G>C