Canonical Allele Identifier: CA360409159

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041500T>C (hg19) ; chr5:g.90745683T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745683T>C , CM000667.2:g.90745683T>C	GRCh38
NC_000005.9:g.90041500T>C , CM000667.1:g.90041500T>C	GRCh37
NC_000005.8:g.90077256T>C	NCBI36
NG_007083.1:g.191884T>C
NG_007083.2:g.221340T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10862T>C MANE Select	ENSP00000384582.2:p.Phe3621Ser
ENST00000639431.1:c.265+69474T>C	ENSP00000491057.1:n.265+69474T>C
ENST00000640374.1:n.4006T>C
ENST00000640464.1:n.1281T>C
ENST00000405460.6:c.10862T>C	ENSP00000384582.2:p.Phe3621Ser
ENST00000509621.1:c.3559T>C
NM_032119.3:c.10862T>C	NP_115495.3:p.Phe3621Ser
NR_003149.1:n.10875T>C
XM_011543675.1:c.10859T>C	XP_011541977.1:p.Phe3620Ser
XM_011543676.1:c.10781T>C	XP_011541978.1:p.Phe3594Ser
XM_011543677.1:c.8165T>C	XP_011541979.1:p.Phe2722Ser
XM_011543678.1:c.10862T>C	XP_011541980.1:p.Phe3621Ser
XM_011543679.1:c.*84T>C	XP_011541981.1:n.*84T>C
NM_032119.4:c.10862T>C MANE Select	NP_115495.3:p.Phe3621Ser
XM_017009963.2:c.10883T>C	XP_016865452.1:p.Phe3628Ser
XM_017009964.2:c.10880T>C	XP_016865453.1:p.Phe3627Ser
XM_017009965.1:c.10880T>C	XP_016865454.1:p.Phe3627Ser
XM_017009966.2:c.10802T>C	XP_016865455.1:p.Phe3601Ser
XM_017009967.1:c.10787T>C	XP_016865456.1:p.Phe3596Ser
XM_017009968.2:c.10883T>C	XP_016865457.1:p.Phe3628Ser
XM_017009969.2:c.10883T>C	XP_016865458.1:p.Phe3628Ser
XM_017009970.2:c.10883T>C	XP_016865459.1:p.Phe3628Ser
XM_017009971.2:c.10883T>C	XP_016865460.1:p.Phe3628Ser
XM_017009972.1:c.4001T>C	XP_016865461.1:p.Phe1334Ser
XM_017009973.1:c.3980T>C	XP_016865462.1:p.Phe1327Ser
XM_017009974.2:c.*84T>C	XP_016865463.1:n.*84T>C
NR_003149.2:n.10878T>C