Canonical Allele Identifier: CA360430858
Community Standard Title: NM_032119.4(ADGRV1):c.17645A>G (p.Tyr5882Cys)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90855791A>G , CM000667.2:g.90855791A>G GRCh38
NC_000005.9:g.90151608A>G , CM000667.1:g.90151608A>G GRCh37
NC_000005.8:g.90187364A>G NCBI36
NG_007083.1:g.301992A>G
NG_007083.2:g.331448A>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.17645A>G MANE Select NP_115495.3:p.Tyr5882Cys
ENST00000405460.9:c.17645A>G MANE Select ENSP00000384582.2:p.Tyr5882Cys
NM_032119.3:c.17645A>G NP_115495.3:p.Tyr5882Cys
NR_003149.1:n.17658A>G
NR_003149.2:n.17661A>G
ENST00000405460.6:c.17645A>G ENSP00000384582.2:p.Tyr5882Cys
ENST00000425867.2:c.4628A>G ENSP00000392618.2:p.Tyr1543Cys
ENST00000425867.3:c.6599A>G ENSP00000392618.3:p.Tyr2200Cys
ENST00000503852.1:n.193A>G
ENST00000638510.1:n.4912A>G
ENST00000638990.1:c.857A>G
ENST00000639431.1:c.266-129553A>G ENSP00000491057.1:n.266-129553A>G
ENST00000640407.1:c.4094A>G ENSP00000491425.1:n.4094A>G
XM_011543675.1:c.17642A>G XP_011541977.1:p.Tyr5881Cys
XM_011543676.1:c.17564A>G XP_011541978.1:p.Tyr5855Cys
XM_011543677.1:c.14948A>G XP_011541979.1:p.Tyr4983Cys
XM_017009963.2:c.17666A>G XP_016865452.1:p.Tyr5889Cys
XM_017009964.2:c.17663A>G XP_016865453.1:p.Tyr5888Cys
XM_017009965.1:c.17663A>G XP_016865454.1:p.Tyr5888Cys
XM_017009966.2:c.17585A>G XP_016865455.1:p.Tyr5862Cys
XM_017009967.1:c.17570A>G XP_016865456.1:p.Tyr5857Cys
XM_017009968.2:c.17486A>G XP_016865457.1:p.Tyr5829Cys
XM_017009969.2:c.17666A>G XP_016865458.1:p.Tyr5889Cys
XM_017009972.1:c.10784A>G XP_016865461.1:p.Tyr3595Cys
XM_017009973.1:c.10763A>G XP_016865462.1:p.Tyr3588Cys