Canonical Allele Identifier: CA360408587
Community Standard Title: NM_032119.4(ADGRV1):c.15244C>T (p.Gln5082Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90810504C>T , CM000667.2:g.90810504C>T GRCh38
NC_000005.9:g.90106321C>T , CM000667.1:g.90106321C>T GRCh37
NC_000005.8:g.90142077C>T NCBI36
NG_007083.1:g.256705C>T
NG_007083.2:g.286161C>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.15244C>T MANE Select NP_115495.3:p.Gln5082Ter
ENST00000405460.9:c.15244C>T MANE Select ENSP00000384582.2:p.Gln5082Ter
NM_032119.3:c.15244C>T NP_115495.3:p.Gln5082Ter
NR_003149.1:n.15257C>T
NR_003149.2:n.15260C>T
ENST00000405460.6:c.15244C>T ENSP00000384582.2:p.Gln5082Ter
ENST00000425867.2:c.2227C>T ENSP00000392618.2:p.Gln743Ter
ENST00000425867.3:c.4198C>T ENSP00000392618.3:p.Gln1400Ter
ENST00000638510.1:n.2511C>T
ENST00000639431.1:c.265+134295C>T ENSP00000491057.1:n.265+134295C>T
ENST00000640407.1:c.1654C>T ENSP00000491425.1:p.Gln552Ter
XM_011543675.1:c.15241C>T XP_011541977.1:p.Gln5081Ter
XM_011543676.1:c.15163C>T XP_011541978.1:p.Gln5055Ter
XM_011543677.1:c.12547C>T XP_011541979.1:p.Gln4183Ter
XM_017009963.2:c.15265C>T XP_016865452.1:p.Gln5089Ter
XM_017009964.2:c.15262C>T XP_016865453.1:p.Gln5088Ter
XM_017009965.1:c.15262C>T XP_016865454.1:p.Gln5088Ter
XM_017009966.2:c.15184C>T XP_016865455.1:p.Gln5062Ter
XM_017009967.1:c.15169C>T XP_016865456.1:p.Gln5057Ter
XM_017009968.2:c.15085C>T XP_016865457.1:p.Gln5029Ter
XM_017009969.2:c.15265C>T XP_016865458.1:p.Gln5089Ter
XM_017009971.2:c.*198C>T XP_016865460.1:n.*198C>T
XM_017009972.1:c.8383C>T XP_016865461.1:p.Gln2795Ter
XM_017009973.1:c.8362C>T XP_016865462.1:p.Gln2788Ter