Canonical Allele Identifier: CA360399097

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90085646A>T (hg19) ; chr5:g.90789829A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789829A>T , CM000667.2:g.90789829A>T	GRCh38
NC_000005.9:g.90085646A>T , CM000667.1:g.90085646A>T	GRCh37
NC_000005.8:g.90121402A>T	NCBI36
NG_007083.1:g.236030A>T
NG_007083.2:g.265486A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14021A>T MANE Select	ENSP00000384582.2:p.Lys4674Met
ENST00000425867.3:c.2975A>T	ENSP00000392618.3:p.Lys992Met
ENST00000638510.1:n.1288A>T
ENST00000638975.1:c.650A>T	ENSP00000492630.1:p.Lys217Met
ENST00000639431.1:c.265+113620A>T	ENSP00000491057.1:n.265+113620A>T
ENST00000640407.1:c.431A>T	ENSP00000491425.1:p.Lys144Met
ENST00000405460.6:c.14021A>T	ENSP00000384582.2:p.Lys4674Met
ENST00000425867.2:c.1004A>T	ENSP00000392618.2:p.Lys335Met
NM_032119.3:c.14021A>T	NP_115495.3:p.Lys4674Met
NR_003149.1:n.14034A>T
XM_011543675.1:c.14018A>T	XP_011541977.1:p.Lys4673Met
XM_011543676.1:c.13940A>T	XP_011541978.1:p.Lys4647Met
XM_011543677.1:c.11324A>T	XP_011541979.1:p.Lys3775Met
XM_011543678.1:c.14021A>T	XP_011541980.1:p.Lys4674Met
NM_032119.4:c.14021A>T MANE Select	NP_115495.3:p.Lys4674Met
XM_017009963.2:c.14042A>T	XP_016865452.1:p.Lys4681Met
XM_017009964.2:c.14039A>T	XP_016865453.1:p.Lys4680Met
XM_017009965.1:c.14039A>T	XP_016865454.1:p.Lys4680Met
XM_017009966.2:c.13961A>T	XP_016865455.1:p.Lys4654Met
XM_017009967.1:c.13946A>T	XP_016865456.1:p.Lys4649Met
XM_017009968.2:c.14042A>T	XP_016865457.1:p.Lys4681Met
XM_017009969.2:c.14042A>T	XP_016865458.1:p.Lys4681Met
XM_017009970.2:c.14042A>T	XP_016865459.1:p.Lys4681Met
XM_017009971.2:c.14042A>T	XP_016865460.1:p.Lys4681Met
XM_017009972.1:c.7160A>T	XP_016865461.1:p.Lys2387Met
XM_017009973.1:c.7139A>T	XP_016865462.1:p.Lys2380Met
NR_003149.2:n.14037A>T