Canonical Allele Identifier: CA360414242

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89979893A>C (hg19) ; chr5:g.90684076A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684076A>C , CM000667.2:g.90684076A>C	GRCh38
NC_000005.9:g.89979893A>C , CM000667.1:g.89979893A>C	GRCh37
NC_000005.8:g.90015649A>C	NCBI36
NG_007083.1:g.130277A>C
NG_007083.2:g.159733A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6155A>C MANE Select	ENSP00000384582.2:p.Asn2052Thr
ENST00000639431.1:c.265+7867A>C	ENSP00000491057.1:n.265+7867A>C
ENST00000639473.1:n.1614A>C
ENST00000640012.1:c.165-1704A>C
ENST00000640403.1:c.3446A>C	ENSP00000492531.1:p.Asn1149Thr
ENST00000640779.1:c.967A>C
ENST00000405460.6:c.6155A>C	ENSP00000384582.2:p.Asn2052Thr
NM_032119.3:c.6155A>C	NP_115495.3:p.Asn2052Thr
NR_003149.1:n.6251A>C
XM_011543675.1:c.6152A>C	XP_011541977.1:p.Asn2051Thr
XM_011543676.1:c.6074A>C	XP_011541978.1:p.Asn2025Thr
XM_011543677.1:c.3458A>C	XP_011541979.1:p.Asn1153Thr
XM_011543678.1:c.6155A>C	XP_011541980.1:p.Asn2052Thr
XM_011543679.1:c.6155A>C	XP_011541981.1:p.Asn2052Thr
NM_032119.4:c.6155A>C MANE Select	NP_115495.3:p.Asn2052Thr
XM_017009963.2:c.6155A>C	XP_016865452.1:p.Asn2052Thr
XM_017009964.2:c.6152A>C	XP_016865453.1:p.Asn2051Thr
XM_017009965.1:c.6152A>C	XP_016865454.1:p.Asn2051Thr
XM_017009966.2:c.6074A>C	XP_016865455.1:p.Asn2025Thr
XM_017009967.1:c.6059A>C	XP_016865456.1:p.Asn2020Thr
XM_017009968.2:c.6155A>C	XP_016865457.1:p.Asn2052Thr
XM_017009969.2:c.6155A>C	XP_016865458.1:p.Asn2052Thr
XM_017009970.2:c.6155A>C	XP_016865459.1:p.Asn2052Thr
XM_017009971.2:c.6155A>C	XP_016865460.1:p.Asn2052Thr
XM_017009973.1:c.-645A>C	XP_016865462.1:n.-645A>C
XM_017009974.2:c.6155A>C	XP_016865463.1:p.Asn2052Thr
NR_003149.2:n.6254A>C