Canonical Allele Identifier: CA360425437

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119242G>C (hg19) ; chr5:g.90823425G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823425G>C , CM000667.2:g.90823425G>C	GRCh38
NC_000005.9:g.90119242G>C , CM000667.1:g.90119242G>C	GRCh37
NC_000005.8:g.90154998G>C	NCBI36
NG_007083.1:g.269626G>C
NG_007083.2:g.299082G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16197G>C MANE Select	ENSP00000384582.2:p.Arg5399Ser
ENST00000425867.3:c.5151G>C	ENSP00000392618.3:p.Arg1717Ser
ENST00000638510.1:n.3464G>C
ENST00000639431.1:c.265+147216G>C	ENSP00000491057.1:n.265+147216G>C
ENST00000640061.1:n.128+1243G>C
ENST00000640407.1:c.2607G>C	ENSP00000491425.1:p.Arg869Ser
ENST00000405460.6:c.16197G>C	ENSP00000384582.2:p.Arg5399Ser
ENST00000425867.2:c.3180G>C	ENSP00000392618.2:p.Arg1060Ser
NM_032119.3:c.16197G>C	NP_115495.3:p.Arg5399Ser
NR_003149.1:n.16210G>C
XM_011543675.1:c.16194G>C	XP_011541977.1:p.Arg5398Ser
XM_011543676.1:c.16116G>C	XP_011541978.1:p.Arg5372Ser
XM_011543677.1:c.13500G>C	XP_011541979.1:p.Arg4500Ser
NM_032119.4:c.16197G>C MANE Select	NP_115495.3:p.Arg5399Ser
XM_017009963.2:c.16218G>C	XP_016865452.1:p.Arg5406Ser
XM_017009964.2:c.16215G>C	XP_016865453.1:p.Arg5405Ser
XM_017009965.1:c.16215G>C	XP_016865454.1:p.Arg5405Ser
XM_017009966.2:c.16137G>C	XP_016865455.1:p.Arg5379Ser
XM_017009967.1:c.16122G>C	XP_016865456.1:p.Arg5374Ser
XM_017009968.2:c.16038G>C	XP_016865457.1:p.Arg5346Ser
XM_017009969.2:c.16218G>C	XP_016865458.1:p.Arg5406Ser
XM_017009972.1:c.9336G>C	XP_016865461.1:p.Arg3112Ser
XM_017009973.1:c.9315G>C	XP_016865462.1:p.Arg3105Ser
NR_003149.2:n.16213G>C