Canonical Allele Identifier: CA360377459

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059165A>T (hg19) ; chr5:g.90763348A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763348A>T , CM000667.2:g.90763348A>T	GRCh38
NC_000005.9:g.90059165A>T , CM000667.1:g.90059165A>T	GRCh37
NC_000005.8:g.90094921A>T	NCBI36
NG_007083.1:g.209549A>T
NG_007083.2:g.239005A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12164A>T MANE Select	ENSP00000384582.2:p.Tyr4055Phe
ENST00000425867.3:c.1118A>T	ENSP00000392618.3:p.Tyr373Phe
ENST00000639431.1:c.265+87139A>T	ENSP00000491057.1:n.265+87139A>T
ENST00000640464.1:n.2583A>T
ENST00000640729.1:n.741A>T
ENST00000405460.6:c.12164A>T	ENSP00000384582.2:p.Tyr4055Phe
NM_032119.3:c.12164A>T	NP_115495.3:p.Tyr4055Phe
NR_003149.1:n.12177A>T
XM_011543675.1:c.12161A>T	XP_011541977.1:p.Tyr4054Phe
XM_011543676.1:c.12083A>T	XP_011541978.1:p.Tyr4028Phe
XM_011543677.1:c.9467A>T	XP_011541979.1:p.Tyr3156Phe
XM_011543678.1:c.12164A>T	XP_011541980.1:p.Tyr4055Phe
NM_032119.4:c.12164A>T MANE Select	NP_115495.3:p.Tyr4055Phe
XM_017009963.2:c.12185A>T	XP_016865452.1:p.Tyr4062Phe
XM_017009964.2:c.12182A>T	XP_016865453.1:p.Tyr4061Phe
XM_017009965.1:c.12182A>T	XP_016865454.1:p.Tyr4061Phe
XM_017009966.2:c.12104A>T	XP_016865455.1:p.Tyr4035Phe
XM_017009967.1:c.12089A>T	XP_016865456.1:p.Tyr4030Phe
XM_017009968.2:c.12185A>T	XP_016865457.1:p.Tyr4062Phe
XM_017009969.2:c.12185A>T	XP_016865458.1:p.Tyr4062Phe
XM_017009970.2:c.12185A>T	XP_016865459.1:p.Tyr4062Phe
XM_017009971.2:c.12185A>T	XP_016865460.1:p.Tyr4062Phe
XM_017009972.1:c.5303A>T	XP_016865461.1:p.Tyr1768Phe
XM_017009973.1:c.5282A>T	XP_016865462.1:p.Tyr1761Phe
NR_003149.2:n.12180A>T