Canonical Allele Identifier: CA360365655
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90627289T>G , CM000667.2:g.90627289T>G GRCh38
NC_000005.9:g.89923106T>G , CM000667.1:g.89923106T>G GRCh37
NC_000005.8:g.89958862T>G NCBI36
NG_007083.1:g.73490T>G
NG_007083.2:g.102946T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.751T>G MANE Select ENSP00000384582.2:p.Ser251Ala
ENST00000640083.1:n.456T>G
ENST00000640109.1:n.847T>G
ENST00000640281.1:n.810T>G
ENST00000405460.6:c.751T>G ENSP00000384582.2:p.Ser251Ala
NM_032119.3:c.751T>G NP_115495.3:p.Ser251Ala
NR_003149.1:n.847T>G
XM_011543675.1:c.751T>G XP_011541977.1:p.Ser251Ala
XM_011543676.1:c.751T>G XP_011541978.1:p.Ser251Ala
XM_011543678.1:c.751T>G XP_011541980.1:p.Ser251Ala
XM_011543679.1:c.751T>G XP_011541981.1:p.Ser251Ala
NM_032119.4:c.751T>G MANE Select NP_115495.3:p.Ser251Ala
XM_017009963.2:c.751T>G XP_016865452.1:p.Ser251Ala
XM_017009964.2:c.751T>G XP_016865453.1:p.Ser251Ala
XM_017009965.1:c.748T>G XP_016865454.1:p.Ser250Ala
XM_017009966.2:c.751T>G XP_016865455.1:p.Ser251Ala
XM_017009967.1:c.655T>G XP_016865456.1:p.Ser219Ala
XM_017009968.2:c.751T>G XP_016865457.1:p.Ser251Ala
XM_017009969.2:c.751T>G XP_016865458.1:p.Ser251Ala
XM_017009970.2:c.751T>G XP_016865459.1:p.Ser251Ala
XM_017009971.2:c.751T>G XP_016865460.1:p.Ser251Ala
XM_017009974.2:c.751T>G XP_016865463.1:p.Ser251Ala
NR_003149.2:n.850T>G