Canonical Allele Identifier: CA445404514

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988508T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692691T>C , CM000667.2:g.90692691T>C	GRCh38
NC_000005.9:g.89988508T>C , CM000667.1:g.89988508T>C	GRCh37
NC_000005.8:g.90024264T>C	NCBI36
NG_007083.1:g.138892T>C
NG_007083.2:g.168348T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7038T>C MANE Select	ENSP00000384582.2:p.Asp2346=
ENST00000639431.1:c.265+16482T>C	ENSP00000491057.1:n.265+16482T>C
ENST00000639473.1:n.2497T>C
ENST00000640012.1:c.845T>C
ENST00000640374.1:n.182T>C
ENST00000640403.1:c.4329T>C	ENSP00000492531.1:p.Asp1443=
ENST00000640779.1:c.1767T>C
ENST00000405460.6:c.7038T>C	ENSP00000384582.2:p.Asp2346=
NM_032119.3:c.7038T>C	NP_115495.3:p.Asp2346=
NR_003149.1:n.7051T>C
XM_011543675.1:c.7035T>C	XP_011541977.1:p.Asp2345=
XM_011543676.1:c.6957T>C	XP_011541978.1:p.Asp2319=
XM_011543677.1:c.4341T>C	XP_011541979.1:p.Asp1447=
XM_011543678.1:c.7038T>C	XP_011541980.1:p.Asp2346=
XM_011543679.1:c.7038T>C	XP_011541981.1:p.Asp2346=
NM_032119.4:c.7038T>C MANE Select	NP_115495.3:p.Asp2346=
XM_017009963.2:c.7038T>C	XP_016865452.1:p.Asp2346=
XM_017009964.2:c.7035T>C	XP_016865453.1:p.Asp2345=
XM_017009965.1:c.7035T>C	XP_016865454.1:p.Asp2345=
XM_017009966.2:c.6957T>C	XP_016865455.1:p.Asp2319=
XM_017009967.1:c.6942T>C	XP_016865456.1:p.Asp2314=
XM_017009968.2:c.7038T>C	XP_016865457.1:p.Asp2346=
XM_017009969.2:c.7038T>C	XP_016865458.1:p.Asp2346=
XM_017009970.2:c.7038T>C	XP_016865459.1:p.Asp2346=
XM_017009971.2:c.7038T>C	XP_016865460.1:p.Asp2346=
XM_017009972.1:c.156T>C	XP_016865461.1:p.Asp52=
XM_017009973.1:c.156T>C	XP_016865462.1:p.Asp52=
XM_017009974.2:c.7038T>C	XP_016865463.1:p.Asp2346=
NR_003149.2:n.7054T>C