Canonical Allele Identifier: CA360377457

Gene: ADGRV1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12164A>C MANE Select	ENSP00000384582.2:p.Tyr4055Ser
ENST00000425867.3:c.1118A>C	ENSP00000392618.3:p.Tyr373Ser
ENST00000639431.1:c.265+87139A>C	ENSP00000491057.1:n.265+87139A>C
ENST00000640464.1:n.2583A>C
ENST00000640729.1:n.741A>C
ENST00000405460.6:c.12164A>C	ENSP00000384582.2:p.Tyr4055Ser
NM_032119.3:c.12164A>C	NP_115495.3:p.Tyr4055Ser
NR_003149.1:n.12177A>C
XM_011543675.1:c.12161A>C	XP_011541977.1:p.Tyr4054Ser
XM_011543676.1:c.12083A>C	XP_011541978.1:p.Tyr4028Ser
XM_011543677.1:c.9467A>C	XP_011541979.1:p.Tyr3156Ser
XM_011543678.1:c.12164A>C	XP_011541980.1:p.Tyr4055Ser
NM_032119.4:c.12164A>C MANE Select	NP_115495.3:p.Tyr4055Ser
XM_017009963.2:c.12185A>C	XP_016865452.1:p.Tyr4062Ser
XM_017009964.2:c.12182A>C	XP_016865453.1:p.Tyr4061Ser
XM_017009965.1:c.12182A>C	XP_016865454.1:p.Tyr4061Ser
XM_017009966.2:c.12104A>C	XP_016865455.1:p.Tyr4035Ser
XM_017009967.1:c.12089A>C	XP_016865456.1:p.Tyr4030Ser
XM_017009968.2:c.12185A>C	XP_016865457.1:p.Tyr4062Ser
XM_017009969.2:c.12185A>C	XP_016865458.1:p.Tyr4062Ser
XM_017009970.2:c.12185A>C	XP_016865459.1:p.Tyr4062Ser
XM_017009971.2:c.12185A>C	XP_016865460.1:p.Tyr4062Ser
XM_017009972.1:c.5303A>C	XP_016865461.1:p.Tyr1768Ser
XM_017009973.1:c.5282A>C	XP_016865462.1:p.Tyr1761Ser
NR_003149.2:n.12180A>C