Canonical Allele Identifier: CA360425472

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119256T>C (hg19) ; chr5:g.90823439T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823439T>C , CM000667.2:g.90823439T>C	GRCh38
NC_000005.9:g.90119256T>C , CM000667.1:g.90119256T>C	GRCh37
NC_000005.8:g.90155012T>C	NCBI36
NG_007083.1:g.269640T>C
NG_007083.2:g.299096T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16211T>C MANE Select	ENSP00000384582.2:p.Val5404Ala
ENST00000425867.3:c.5165T>C	ENSP00000392618.3:p.Val1722Ala
ENST00000638510.1:n.3478T>C
ENST00000639431.1:c.265+147230T>C	ENSP00000491057.1:n.265+147230T>C
ENST00000640061.1:n.128+1257T>C
ENST00000640407.1:c.2621T>C	ENSP00000491425.1:p.Val874Ala
ENST00000405460.6:c.16211T>C	ENSP00000384582.2:p.Val5404Ala
ENST00000425867.2:c.3194T>C	ENSP00000392618.2:p.Val1065Ala
NM_032119.3:c.16211T>C	NP_115495.3:p.Val5404Ala
NR_003149.1:n.16224T>C
XM_011543675.1:c.16208T>C	XP_011541977.1:p.Val5403Ala
XM_011543676.1:c.16130T>C	XP_011541978.1:p.Val5377Ala
XM_011543677.1:c.13514T>C	XP_011541979.1:p.Val4505Ala
NM_032119.4:c.16211T>C MANE Select	NP_115495.3:p.Val5404Ala
XM_017009963.2:c.16232T>C	XP_016865452.1:p.Val5411Ala
XM_017009964.2:c.16229T>C	XP_016865453.1:p.Val5410Ala
XM_017009965.1:c.16229T>C	XP_016865454.1:p.Val5410Ala
XM_017009966.2:c.16151T>C	XP_016865455.1:p.Val5384Ala
XM_017009967.1:c.16136T>C	XP_016865456.1:p.Val5379Ala
XM_017009968.2:c.16052T>C	XP_016865457.1:p.Val5351Ala
XM_017009969.2:c.16232T>C	XP_016865458.1:p.Val5411Ala
XM_017009972.1:c.9350T>C	XP_016865461.1:p.Val3117Ala
XM_017009973.1:c.9329T>C	XP_016865462.1:p.Val3110Ala
NR_003149.2:n.16227T>C