Canonical Allele Identifier: CA360410340

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106715A>C (hg19) ; chr5:g.90810898A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810898A>C , CM000667.2:g.90810898A>C	GRCh38
NC_000005.9:g.90106715A>C , CM000667.1:g.90106715A>C	GRCh37
NC_000005.8:g.90142471A>C	NCBI36
NG_007083.1:g.257099A>C
NG_007083.2:g.286555A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15638A>C MANE Select	ENSP00000384582.2:p.Asn5213Thr
ENST00000425867.3:c.4592A>C	ENSP00000392618.3:p.Asn1531Thr
ENST00000638510.1:n.2905A>C
ENST00000639431.1:c.265+134689A>C	ENSP00000491057.1:n.265+134689A>C
ENST00000640407.1:c.2048A>C	ENSP00000491425.1:p.Asn683Thr
ENST00000405460.6:c.15638A>C	ENSP00000384582.2:p.Asn5213Thr
ENST00000425867.2:c.2621A>C	ENSP00000392618.2:p.Asn874Thr
NM_032119.3:c.15638A>C	NP_115495.3:p.Asn5213Thr
NR_003149.1:n.15651A>C
XM_011543675.1:c.15635A>C	XP_011541977.1:p.Asn5212Thr
XM_011543676.1:c.15557A>C	XP_011541978.1:p.Asn5186Thr
XM_011543677.1:c.12941A>C	XP_011541979.1:p.Asn4314Thr
NM_032119.4:c.15638A>C MANE Select	NP_115495.3:p.Asn5213Thr
XM_017009963.2:c.15659A>C	XP_016865452.1:p.Asn5220Thr
XM_017009964.2:c.15656A>C	XP_016865453.1:p.Asn5219Thr
XM_017009965.1:c.15656A>C	XP_016865454.1:p.Asn5219Thr
XM_017009966.2:c.15578A>C	XP_016865455.1:p.Asn5193Thr
XM_017009967.1:c.15563A>C	XP_016865456.1:p.Asn5188Thr
XM_017009968.2:c.15479A>C	XP_016865457.1:p.Asn5160Thr
XM_017009969.2:c.15659A>C	XP_016865458.1:p.Asn5220Thr
XM_017009972.1:c.8777A>C	XP_016865461.1:p.Asn2926Thr
XM_017009973.1:c.8756A>C	XP_016865462.1:p.Asn2919Thr
NR_003149.2:n.15654A>C