Canonical Allele Identifier: CA3341601
Community Standard Title: NM_032119.4(ADGRV1):c.13742A>G (p.Tyr4581Cys)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90788159A>G , CM000667.2:g.90788159A>G GRCh38
NC_000005.9:g.90083976A>G , CM000667.1:g.90083976A>G GRCh37
NC_000005.8:g.90119732A>G NCBI36
NG_007083.1:g.234360A>G
NG_007083.2:g.263816A>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.13742A>G MANE Select NP_115495.3:p.Tyr4581Cys
ENST00000405460.9:c.13742A>G MANE Select ENSP00000384582.2:p.Tyr4581Cys
NM_032119.3:c.13742A>G NP_115495.3:p.Tyr4581Cys
NR_003149.1:n.13755A>G
NR_003149.2:n.13758A>G
ENST00000405460.6:c.13742A>G ENSP00000384582.2:p.Tyr4581Cys
ENST00000425867.2:c.725A>G ENSP00000392618.2:p.Tyr242Cys
ENST00000425867.3:c.2696A>G ENSP00000392618.3:p.Tyr899Cys
ENST00000638510.1:n.1009A>G
ENST00000638975.1:c.371A>G ENSP00000492630.1:p.Tyr124Cys
ENST00000639431.1:c.265+111950A>G ENSP00000491057.1:n.265+111950A>G
ENST00000640407.1:c.152A>G ENSP00000491425.1:p.Tyr51Cys
XM_011543675.1:c.13739A>G XP_011541977.1:p.Tyr4580Cys
XM_011543676.1:c.13661A>G XP_011541978.1:p.Tyr4554Cys
XM_011543677.1:c.11045A>G XP_011541979.1:p.Tyr3682Cys
XM_011543678.1:c.13742A>G XP_011541980.1:p.Tyr4581Cys
XM_017009963.2:c.13763A>G XP_016865452.1:p.Tyr4588Cys
XM_017009964.2:c.13760A>G XP_016865453.1:p.Tyr4587Cys
XM_017009965.1:c.13760A>G XP_016865454.1:p.Tyr4587Cys
XM_017009966.2:c.13682A>G XP_016865455.1:p.Tyr4561Cys
XM_017009967.1:c.13667A>G XP_016865456.1:p.Tyr4556Cys
XM_017009968.2:c.13763A>G XP_016865457.1:p.Tyr4588Cys
XM_017009969.2:c.13763A>G XP_016865458.1:p.Tyr4588Cys
XM_017009970.2:c.13763A>G XP_016865459.1:p.Tyr4588Cys
XM_017009971.2:c.13763A>G XP_016865460.1:p.Tyr4588Cys
XM_017009972.1:c.6881A>G XP_016865461.1:p.Tyr2294Cys
XM_017009973.1:c.6860A>G XP_016865462.1:p.Tyr2287Cys