Canonical Allele Identifier: CA360397603

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012482A>C (hg19) ; chr5:g.90716665A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716665A>C , CM000667.2:g.90716665A>C	GRCh38
NC_000005.9:g.90012482A>C , CM000667.1:g.90012482A>C	GRCh37
NC_000005.8:g.90048238A>C	NCBI36
NG_007083.1:g.162866A>C
NG_007083.2:g.192322A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9383A>C MANE Select	ENSP00000384582.2:p.Asn3128Thr
ENST00000639431.1:c.265+40456A>C	ENSP00000491057.1:n.265+40456A>C
ENST00000639473.1:n.4842A>C
ENST00000640012.1:c.3190A>C
ENST00000640374.1:n.2527A>C
ENST00000640779.1:c.4112A>C
ENST00000405460.6:c.9383A>C	ENSP00000384582.2:p.Asn3128Thr
ENST00000509621.1:c.2080A>C
NM_032119.3:c.9383A>C	NP_115495.3:p.Asn3128Thr
NR_003149.1:n.9396A>C
XM_011543675.1:c.9380A>C	XP_011541977.1:p.Asn3127Thr
XM_011543676.1:c.9302A>C	XP_011541978.1:p.Asn3101Thr
XM_011543677.1:c.6686A>C	XP_011541979.1:p.Asn2229Thr
XM_011543678.1:c.9383A>C	XP_011541980.1:p.Asn3128Thr
XM_011543679.1:c.9383A>C	XP_011541981.1:p.Asn3128Thr
XR_948560.1:n.272-856T>G
NM_032119.4:c.9383A>C MANE Select	NP_115495.3:p.Asn3128Thr
XM_017009963.2:c.9404A>C	XP_016865452.1:p.Asn3135Thr
XM_017009964.2:c.9401A>C	XP_016865453.1:p.Asn3134Thr
XM_017009965.1:c.9401A>C	XP_016865454.1:p.Asn3134Thr
XM_017009966.2:c.9323A>C	XP_016865455.1:p.Asn3108Thr
XM_017009967.1:c.9308A>C	XP_016865456.1:p.Asn3103Thr
XM_017009968.2:c.9404A>C	XP_016865457.1:p.Asn3135Thr
XM_017009969.2:c.9404A>C	XP_016865458.1:p.Asn3135Thr
XM_017009970.2:c.9404A>C	XP_016865459.1:p.Asn3135Thr
XM_017009971.2:c.9404A>C	XP_016865460.1:p.Asn3135Thr
XM_017009972.1:c.2522A>C	XP_016865461.1:p.Asn841Thr
XM_017009973.1:c.2501A>C	XP_016865462.1:p.Asn834Thr
XM_017009974.2:c.9404A>C	XP_016865463.1:p.Asn3135Thr
XR_001742802.1:n.2523-856T>G
NR_003149.2:n.9399A>C