Canonical Allele Identifier: CA360425550

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119298T>C (hg19) ; chr5:g.90823481T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823481T>C , CM000667.2:g.90823481T>C	GRCh38
NC_000005.9:g.90119298T>C , CM000667.1:g.90119298T>C	GRCh37
NC_000005.8:g.90155054T>C	NCBI36
NG_007083.1:g.269682T>C
NG_007083.2:g.299138T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16253T>C MANE Select	ENSP00000384582.2:p.Val5418Ala
ENST00000425867.3:c.5207T>C	ENSP00000392618.3:p.Val1736Ala
ENST00000638510.1:n.3520T>C
ENST00000639431.1:c.265+147272T>C	ENSP00000491057.1:n.265+147272T>C
ENST00000640061.1:n.128+1299T>C
ENST00000640407.1:c.2663T>C	ENSP00000491425.1:p.Val888Ala
ENST00000405460.6:c.16253T>C	ENSP00000384582.2:p.Val5418Ala
ENST00000425867.2:c.3236T>C	ENSP00000392618.2:p.Val1079Ala
NM_032119.3:c.16253T>C	NP_115495.3:p.Val5418Ala
NR_003149.1:n.16266T>C
XM_011543675.1:c.16250T>C	XP_011541977.1:p.Val5417Ala
XM_011543676.1:c.16172T>C	XP_011541978.1:p.Val5391Ala
XM_011543677.1:c.13556T>C	XP_011541979.1:p.Val4519Ala
NM_032119.4:c.16253T>C MANE Select	NP_115495.3:p.Val5418Ala
XM_017009963.2:c.16274T>C	XP_016865452.1:p.Val5425Ala
XM_017009964.2:c.16271T>C	XP_016865453.1:p.Val5424Ala
XM_017009965.1:c.16271T>C	XP_016865454.1:p.Val5424Ala
XM_017009966.2:c.16193T>C	XP_016865455.1:p.Val5398Ala
XM_017009967.1:c.16178T>C	XP_016865456.1:p.Val5393Ala
XM_017009968.2:c.16094T>C	XP_016865457.1:p.Val5365Ala
XM_017009969.2:c.16274T>C	XP_016865458.1:p.Val5425Ala
XM_017009972.1:c.9392T>C	XP_016865461.1:p.Val3131Ala
XM_017009973.1:c.9371T>C	XP_016865462.1:p.Val3124Ala
NR_003149.2:n.16269T>C