Canonical Allele Identifier: CA360377451

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059164T>G (hg19) ; chr5:g.90763347T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763347T>G , CM000667.2:g.90763347T>G	GRCh38
NC_000005.9:g.90059164T>G , CM000667.1:g.90059164T>G	GRCh37
NC_000005.8:g.90094920T>G	NCBI36
NG_007083.1:g.209548T>G
NG_007083.2:g.239004T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12163T>G MANE Select	ENSP00000384582.2:p.Tyr4055Asp
ENST00000425867.3:c.1117T>G	ENSP00000392618.3:p.Tyr373Asp
ENST00000639431.1:c.265+87138T>G	ENSP00000491057.1:n.265+87138T>G
ENST00000640464.1:n.2582T>G
ENST00000640729.1:n.740T>G
ENST00000405460.6:c.12163T>G	ENSP00000384582.2:p.Tyr4055Asp
NM_032119.3:c.12163T>G	NP_115495.3:p.Tyr4055Asp
NR_003149.1:n.12176T>G
XM_011543675.1:c.12160T>G	XP_011541977.1:p.Tyr4054Asp
XM_011543676.1:c.12082T>G	XP_011541978.1:p.Tyr4028Asp
XM_011543677.1:c.9466T>G	XP_011541979.1:p.Tyr3156Asp
XM_011543678.1:c.12163T>G	XP_011541980.1:p.Tyr4055Asp
NM_032119.4:c.12163T>G MANE Select	NP_115495.3:p.Tyr4055Asp
XM_017009963.2:c.12184T>G	XP_016865452.1:p.Tyr4062Asp
XM_017009964.2:c.12181T>G	XP_016865453.1:p.Tyr4061Asp
XM_017009965.1:c.12181T>G	XP_016865454.1:p.Tyr4061Asp
XM_017009966.2:c.12103T>G	XP_016865455.1:p.Tyr4035Asp
XM_017009967.1:c.12088T>G	XP_016865456.1:p.Tyr4030Asp
XM_017009968.2:c.12184T>G	XP_016865457.1:p.Tyr4062Asp
XM_017009969.2:c.12184T>G	XP_016865458.1:p.Tyr4062Asp
XM_017009970.2:c.12184T>G	XP_016865459.1:p.Tyr4062Asp
XM_017009971.2:c.12184T>G	XP_016865460.1:p.Tyr4062Asp
XM_017009972.1:c.5302T>G	XP_016865461.1:p.Tyr1768Asp
XM_017009973.1:c.5281T>G	XP_016865462.1:p.Tyr1761Asp
NR_003149.2:n.12179T>G