Canonical Allele Identifier: CA1562918255
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823468A= , CM000667.2:g.90823468A= GRCh38
NC_000005.9:g.90119285A= , CM000667.1:g.90119285A= GRCh37
NC_000005.8:g.90155041A= NCBI36
NG_007083.1:g.269669A=
NG_007083.2:g.299125A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16240A= MANE Select ENSP00000384582.2:p.Lys5414=
ENST00000425867.3:c.5194A= ENSP00000392618.3:p.Lys1732=
ENST00000638510.1:n.3507A=
ENST00000639431.1:c.265+147259A= ENSP00000491057.1:n.265+147259A=
ENST00000640061.1:n.128+1286A=
ENST00000640407.1:c.2650A= ENSP00000491425.1:p.Lys884=
ENST00000405460.6:c.16240A= ENSP00000384582.2:p.Lys5414=
ENST00000425867.2:c.3223A= ENSP00000392618.2:p.Lys1075=
NM_032119.3:c.16240A= NP_115495.3:p.Lys5414=
NR_003149.1:n.16253A=
XM_011543675.1:c.16237A= XP_011541977.1:p.Lys5413=
XM_011543676.1:c.16159A= XP_011541978.1:p.Lys5387=
XM_011543677.1:c.13543A= XP_011541979.1:p.Lys4515=
NM_032119.4:c.16240A= MANE Select NP_115495.3:p.Lys5414=
XM_017009963.2:c.16261A= XP_016865452.1:p.Lys5421=
XM_017009964.2:c.16258A= XP_016865453.1:p.Lys5420=
XM_017009965.1:c.16258A= XP_016865454.1:p.Lys5420=
XM_017009966.2:c.16180A= XP_016865455.1:p.Lys5394=
XM_017009967.1:c.16165A= XP_016865456.1:p.Lys5389=
XM_017009968.2:c.16081A= XP_016865457.1:p.Lys5361=
XM_017009969.2:c.16261A= XP_016865458.1:p.Lys5421=
XM_017009972.1:c.9379A= XP_016865461.1:p.Lys3127=
XM_017009973.1:c.9358A= XP_016865462.1:p.Lys3120=
NR_003149.2:n.16256A=