Canonical Allele Identifier: CA360397574

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012473A>C (hg19) ; chr5:g.90716656A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716656A>C , CM000667.2:g.90716656A>C	GRCh38
NC_000005.9:g.90012473A>C , CM000667.1:g.90012473A>C	GRCh37
NC_000005.8:g.90048229A>C	NCBI36
NG_007083.1:g.162857A>C
NG_007083.2:g.192313A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9374A>C MANE Select	ENSP00000384582.2:p.Asn3125Thr
ENST00000639431.1:c.265+40447A>C	ENSP00000491057.1:n.265+40447A>C
ENST00000639473.1:n.4833A>C
ENST00000640012.1:c.3181A>C
ENST00000640374.1:n.2518A>C
ENST00000640779.1:c.4103A>C
ENST00000405460.6:c.9374A>C	ENSP00000384582.2:p.Asn3125Thr
ENST00000509621.1:c.2071A>C
NM_032119.3:c.9374A>C	NP_115495.3:p.Asn3125Thr
NR_003149.1:n.9387A>C
XM_011543675.1:c.9371A>C	XP_011541977.1:p.Asn3124Thr
XM_011543676.1:c.9293A>C	XP_011541978.1:p.Asn3098Thr
XM_011543677.1:c.6677A>C	XP_011541979.1:p.Asn2226Thr
XM_011543678.1:c.9374A>C	XP_011541980.1:p.Asn3125Thr
XM_011543679.1:c.9374A>C	XP_011541981.1:p.Asn3125Thr
XR_948560.1:n.272-847T>G
NM_032119.4:c.9374A>C MANE Select	NP_115495.3:p.Asn3125Thr
XM_017009963.2:c.9395A>C	XP_016865452.1:p.Asn3132Thr
XM_017009964.2:c.9392A>C	XP_016865453.1:p.Asn3131Thr
XM_017009965.1:c.9392A>C	XP_016865454.1:p.Asn3131Thr
XM_017009966.2:c.9314A>C	XP_016865455.1:p.Asn3105Thr
XM_017009967.1:c.9299A>C	XP_016865456.1:p.Asn3100Thr
XM_017009968.2:c.9395A>C	XP_016865457.1:p.Asn3132Thr
XM_017009969.2:c.9395A>C	XP_016865458.1:p.Asn3132Thr
XM_017009970.2:c.9395A>C	XP_016865459.1:p.Asn3132Thr
XM_017009971.2:c.9395A>C	XP_016865460.1:p.Asn3132Thr
XM_017009972.1:c.2513A>C	XP_016865461.1:p.Asn838Thr
XM_017009973.1:c.2492A>C	XP_016865462.1:p.Asn831Thr
XM_017009974.2:c.9395A>C	XP_016865463.1:p.Asn3132Thr
XR_001742802.1:n.2523-847T>G
NR_003149.2:n.9390A>C