Canonical Allele Identifier: CA2541249624
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90745677_90745678insG , CM000667.2:g.90745677_90745678insG GRCh38
NC_000005.9:g.90041494_90041495insG , CM000667.1:g.90041494_90041495insG GRCh37
NC_000005.8:g.90077250_90077251insG NCBI36
NG_007083.1:g.191878_191879insG
NG_007083.2:g.221334_221335insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.10856_10857insG MANE Select ENSP00000384582.2:p.Ser3620IlefsTer7
ENST00000639431.1:c.265+69468_265+69469insG ENSP00000491057.1:n.265+69468_265+69469insG
ENST00000640374.1:n.4000_4001insG
ENST00000640464.1:n.1275_1276insG
ENST00000405460.6:c.10856_10857insG ENSP00000384582.2:p.Ser3620IlefsTer7
ENST00000509621.1:c.3553_3554insG
NM_032119.3:c.10856_10857insG NP_115495.3:p.Ser3620IlefsTer7
NR_003149.1:n.10869_10870insG
XM_011543675.1:c.10853_10854insG XP_011541977.1:p.Ser3619IlefsTer7
XM_011543676.1:c.10775_10776insG XP_011541978.1:p.Ser3593IlefsTer7
XM_011543677.1:c.8159_8160insG XP_011541979.1:p.Ser2721IlefsTer7
XM_011543678.1:c.10856_10857insG XP_011541980.1:p.Ser3620IlefsTer7
XM_011543679.1:c.*78_*79insG XP_011541981.1:n.*78_*79insG
NM_032119.4:c.10856_10857insG MANE Select NP_115495.3:p.Ser3620IlefsTer7
XM_017009963.2:c.10877_10878insG XP_016865452.1:p.Ser3627IlefsTer7
XM_017009964.2:c.10874_10875insG XP_016865453.1:p.Ser3626IlefsTer7
XM_017009965.1:c.10874_10875insG XP_016865454.1:p.Ser3626IlefsTer7
XM_017009966.2:c.10796_10797insG XP_016865455.1:p.Ser3600IlefsTer7
XM_017009967.1:c.10781_10782insG XP_016865456.1:p.Ser3595IlefsTer7
XM_017009968.2:c.10877_10878insG XP_016865457.1:p.Ser3627IlefsTer7
XM_017009969.2:c.10877_10878insG XP_016865458.1:p.Ser3627IlefsTer7
XM_017009970.2:c.10877_10878insG XP_016865459.1:p.Ser3627IlefsTer7
XM_017009971.2:c.10877_10878insG XP_016865460.1:p.Ser3627IlefsTer7
XM_017009972.1:c.3995_3996insG XP_016865461.1:p.Ser1333IlefsTer7
XM_017009973.1:c.3974_3975insG XP_016865462.1:p.Ser1326IlefsTer7
XM_017009974.2:c.*78_*79insG XP_016865463.1:n.*78_*79insG
NR_003149.2:n.10872_10873insG