Canonical Allele Identifier: CA360409708
Community Standard Title: NM_032119.4(ADGRV1):c.15480C>A (p.Tyr5160Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90810740C>A , CM000667.2:g.90810740C>A GRCh38
NC_000005.9:g.90106557C>A , CM000667.1:g.90106557C>A GRCh37
NC_000005.8:g.90142313C>A NCBI36
NG_007083.1:g.256941C>A
NG_007083.2:g.286397C>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.15480C>A MANE Select NP_115495.3:p.Tyr5160Ter
ENST00000405460.9:c.15480C>A MANE Select ENSP00000384582.2:p.Tyr5160Ter
NM_032119.3:c.15480C>A NP_115495.3:p.Tyr5160Ter
NR_003149.1:n.15493C>A
NR_003149.2:n.15496C>A
ENST00000405460.6:c.15480C>A ENSP00000384582.2:p.Tyr5160Ter
ENST00000425867.2:c.2463C>A ENSP00000392618.2:p.Tyr821Ter
ENST00000425867.3:c.4434C>A ENSP00000392618.3:p.Tyr1478Ter
ENST00000638510.1:n.2747C>A
ENST00000639431.1:c.265+134531C>A ENSP00000491057.1:n.265+134531C>A
ENST00000640407.1:c.1890C>A ENSP00000491425.1:p.Tyr630Ter
XM_011543675.1:c.15477C>A XP_011541977.1:p.Tyr5159Ter
XM_011543676.1:c.15399C>A XP_011541978.1:p.Tyr5133Ter
XM_011543677.1:c.12783C>A XP_011541979.1:p.Tyr4261Ter
XM_017009963.2:c.15501C>A XP_016865452.1:p.Tyr5167Ter
XM_017009964.2:c.15498C>A XP_016865453.1:p.Tyr5166Ter
XM_017009965.1:c.15498C>A XP_016865454.1:p.Tyr5166Ter
XM_017009966.2:c.15420C>A XP_016865455.1:p.Tyr5140Ter
XM_017009967.1:c.15405C>A XP_016865456.1:p.Tyr5135Ter
XM_017009968.2:c.15321C>A XP_016865457.1:p.Tyr5107Ter
XM_017009969.2:c.15501C>A XP_016865458.1:p.Tyr5167Ter
XM_017009971.2:c.*434C>A XP_016865460.1:n.*434C>A
XM_017009972.1:c.8619C>A XP_016865461.1:p.Tyr2873Ter
XM_017009973.1:c.8598C>A XP_016865462.1:p.Tyr2866Ter