Canonical Allele Identifier: CA360410334

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106714A>C (hg19) ; chr5:g.90810897A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810897A>C , CM000667.2:g.90810897A>C	GRCh38
NC_000005.9:g.90106714A>C , CM000667.1:g.90106714A>C	GRCh37
NC_000005.8:g.90142470A>C	NCBI36
NG_007083.1:g.257098A>C
NG_007083.2:g.286554A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15637A>C MANE Select	ENSP00000384582.2:p.Asn5213His
ENST00000425867.3:c.4591A>C	ENSP00000392618.3:p.Asn1531His
ENST00000638510.1:n.2904A>C
ENST00000639431.1:c.265+134688A>C	ENSP00000491057.1:n.265+134688A>C
ENST00000640407.1:c.2047A>C	ENSP00000491425.1:p.Asn683His
ENST00000405460.6:c.15637A>C	ENSP00000384582.2:p.Asn5213His
ENST00000425867.2:c.2620A>C	ENSP00000392618.2:p.Asn874His
NM_032119.3:c.15637A>C	NP_115495.3:p.Asn5213His
NR_003149.1:n.15650A>C
XM_011543675.1:c.15634A>C	XP_011541977.1:p.Asn5212His
XM_011543676.1:c.15556A>C	XP_011541978.1:p.Asn5186His
XM_011543677.1:c.12940A>C	XP_011541979.1:p.Asn4314His
NM_032119.4:c.15637A>C MANE Select	NP_115495.3:p.Asn5213His
XM_017009963.2:c.15658A>C	XP_016865452.1:p.Asn5220His
XM_017009964.2:c.15655A>C	XP_016865453.1:p.Asn5219His
XM_017009965.1:c.15655A>C	XP_016865454.1:p.Asn5219His
XM_017009966.2:c.15577A>C	XP_016865455.1:p.Asn5193His
XM_017009967.1:c.15562A>C	XP_016865456.1:p.Asn5188His
XM_017009968.2:c.15478A>C	XP_016865457.1:p.Asn5160His
XM_017009969.2:c.15658A>C	XP_016865458.1:p.Asn5220His
XM_017009972.1:c.8776A>C	XP_016865461.1:p.Asn2926His
XM_017009973.1:c.8755A>C	XP_016865462.1:p.Asn2919His
NR_003149.2:n.15653A>C