Canonical Allele Identifier: CA360401258

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086921G>C (hg19) ; chr5:g.90791104G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791104G>C , CM000667.2:g.90791104G>C	GRCh38
NC_000005.9:g.90086921G>C , CM000667.1:g.90086921G>C	GRCh37
NC_000005.8:g.90122677G>C	NCBI36
NG_007083.1:g.237305G>C
NG_007083.2:g.266761G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14275G>C MANE Select	ENSP00000384582.2:p.Asp4759His
ENST00000425867.3:c.3229G>C	ENSP00000392618.3:p.Asp1077His
ENST00000638510.1:n.1542G>C
ENST00000638585.1:n.41G>C
ENST00000638975.1:c.904G>C	ENSP00000492630.1:p.Asp302His
ENST00000639431.1:c.265+114895G>C	ENSP00000491057.1:n.265+114895G>C
ENST00000640407.1:c.685G>C	ENSP00000491425.1:p.Asp229His
ENST00000405460.6:c.14275G>C	ENSP00000384582.2:p.Asp4759His
ENST00000425867.2:c.1258G>C	ENSP00000392618.2:p.Asp420His
NM_032119.3:c.14275G>C	NP_115495.3:p.Asp4759His
NR_003149.1:n.14288G>C
XM_011543675.1:c.14272G>C	XP_011541977.1:p.Asp4758His
XM_011543676.1:c.14194G>C	XP_011541978.1:p.Asp4732His
XM_011543677.1:c.11578G>C	XP_011541979.1:p.Asp3860His
XM_011543678.1:c.14275G>C	XP_011541980.1:p.Asp4759His
NM_032119.4:c.14275G>C MANE Select	NP_115495.3:p.Asp4759His
XM_017009963.2:c.14296G>C	XP_016865452.1:p.Asp4766His
XM_017009964.2:c.14293G>C	XP_016865453.1:p.Asp4765His
XM_017009965.1:c.14293G>C	XP_016865454.1:p.Asp4765His
XM_017009966.2:c.14215G>C	XP_016865455.1:p.Asp4739His
XM_017009967.1:c.14200G>C	XP_016865456.1:p.Asp4734His
XM_017009968.2:c.14296G>C	XP_016865457.1:p.Asp4766His
XM_017009969.2:c.14296G>C	XP_016865458.1:p.Asp4766His
XM_017009970.2:c.14296G>C	XP_016865459.1:p.Asp4766His
XM_017009971.2:c.14296G>C	XP_016865460.1:p.Asp4766His
XM_017009972.1:c.7414G>C	XP_016865461.1:p.Asp2472His
XM_017009973.1:c.7393G>C	XP_016865462.1:p.Asp2465His
NR_003149.2:n.14291G>C