Canonical Allele Identifier: CA360425482

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119261G>C (hg19) ; chr5:g.90823444G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823444G>C , CM000667.2:g.90823444G>C	GRCh38
NC_000005.9:g.90119261G>C , CM000667.1:g.90119261G>C	GRCh37
NC_000005.8:g.90155017G>C	NCBI36
NG_007083.1:g.269645G>C
NG_007083.2:g.299101G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16216G>C MANE Select	ENSP00000384582.2:p.Val5406Leu
ENST00000425867.3:c.5170G>C	ENSP00000392618.3:p.Val1724Leu
ENST00000638510.1:n.3483G>C
ENST00000639431.1:c.265+147235G>C	ENSP00000491057.1:n.265+147235G>C
ENST00000640061.1:n.128+1262G>C
ENST00000640407.1:c.2626G>C	ENSP00000491425.1:p.Val876Leu
ENST00000405460.6:c.16216G>C	ENSP00000384582.2:p.Val5406Leu
ENST00000425867.2:c.3199G>C	ENSP00000392618.2:p.Val1067Leu
NM_032119.3:c.16216G>C	NP_115495.3:p.Val5406Leu
NR_003149.1:n.16229G>C
XM_011543675.1:c.16213G>C	XP_011541977.1:p.Val5405Leu
XM_011543676.1:c.16135G>C	XP_011541978.1:p.Val5379Leu
XM_011543677.1:c.13519G>C	XP_011541979.1:p.Val4507Leu
NM_032119.4:c.16216G>C MANE Select	NP_115495.3:p.Val5406Leu
XM_017009963.2:c.16237G>C	XP_016865452.1:p.Val5413Leu
XM_017009964.2:c.16234G>C	XP_016865453.1:p.Val5412Leu
XM_017009965.1:c.16234G>C	XP_016865454.1:p.Val5412Leu
XM_017009966.2:c.16156G>C	XP_016865455.1:p.Val5386Leu
XM_017009967.1:c.16141G>C	XP_016865456.1:p.Val5381Leu
XM_017009968.2:c.16057G>C	XP_016865457.1:p.Val5353Leu
XM_017009969.2:c.16237G>C	XP_016865458.1:p.Val5413Leu
XM_017009972.1:c.9355G>C	XP_016865461.1:p.Val3119Leu
XM_017009973.1:c.9334G>C	XP_016865462.1:p.Val3112Leu
NR_003149.2:n.16232G>C