Canonical Allele Identifier: CA360366733

Gene: ADGRV1

Linked Data

• dbSNP Id: rs2149973624
• MyVariant Identifiers: chr5:g.90050893T>C (hg19) ; chr5:g.90755076T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755076T>C , CM000667.2:g.90755076T>C	GRCh38
NC_000005.9:g.90050893T>C , CM000667.1:g.90050893T>C	GRCh37
NC_000005.8:g.90086649T>C	NCBI36
NG_007083.1:g.201277T>C
NG_007083.2:g.230733T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11471T>C MANE Select	ENSP00000384582.2:p.Leu3824Pro
ENST00000425867.3:c.602T>C	ENSP00000392618.3:p.Leu201Pro
ENST00000639431.1:c.265+78867T>C	ENSP00000491057.1:n.265+78867T>C
ENST00000640374.1:n.4615T>C
ENST00000640464.1:n.1890T>C
ENST00000405460.6:c.11471T>C	ENSP00000384582.2:p.Leu3824Pro
ENST00000509621.1:c.4168T>C
NM_032119.3:c.11471T>C	NP_115495.3:p.Leu3824Pro
NR_003149.1:n.11484T>C
XM_011543675.1:c.11468T>C	XP_011541977.1:p.Leu3823Pro
XM_011543676.1:c.11390T>C	XP_011541978.1:p.Leu3797Pro
XM_011543677.1:c.8774T>C	XP_011541979.1:p.Leu2925Pro
XM_011543678.1:c.11471T>C	XP_011541980.1:p.Leu3824Pro
NM_032119.4:c.11471T>C MANE Select	NP_115495.3:p.Leu3824Pro
XM_017009963.2:c.11492T>C	XP_016865452.1:p.Leu3831Pro
XM_017009964.2:c.11489T>C	XP_016865453.1:p.Leu3830Pro
XM_017009965.1:c.11489T>C	XP_016865454.1:p.Leu3830Pro
XM_017009966.2:c.11411T>C	XP_016865455.1:p.Leu3804Pro
XM_017009967.1:c.11396T>C	XP_016865456.1:p.Leu3799Pro
XM_017009968.2:c.11492T>C	XP_016865457.1:p.Leu3831Pro
XM_017009969.2:c.11492T>C	XP_016865458.1:p.Leu3831Pro
XM_017009970.2:c.11492T>C	XP_016865459.1:p.Leu3831Pro
XM_017009971.2:c.11492T>C	XP_016865460.1:p.Leu3831Pro
XM_017009972.1:c.4610T>C	XP_016865461.1:p.Leu1537Pro
XM_017009973.1:c.4589T>C	XP_016865462.1:p.Leu1530Pro
NR_003149.2:n.11487T>C