Canonical Allele Identifier: CA3341554
Community Standard Title: NM_032119.4(ADGRV1):c.13568G>C (p.Ser4523Thr)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90783972G>C , CM000667.2:g.90783972G>C GRCh38
NC_000005.9:g.90079789G>C , CM000667.1:g.90079789G>C GRCh37
NC_000005.8:g.90115545G>C NCBI36
NG_007083.1:g.230173G>C
NG_007083.2:g.259629G>C

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.13568G>C MANE Select NP_115495.3:p.Ser4523Thr
ENST00000405460.9:c.13568G>C MANE Select ENSP00000384582.2:p.Ser4523Thr
NM_032119.3:c.13568G>C NP_115495.3:p.Ser4523Thr
NR_003149.1:n.13581G>C
NR_003149.2:n.13584G>C
ENST00000405460.6:c.13568G>C ENSP00000384582.2:p.Ser4523Thr
ENST00000425867.2:c.551G>C ENSP00000392618.2:p.Ser184Thr
ENST00000425867.3:c.2522G>C ENSP00000392618.3:p.Ser841Thr
ENST00000638510.1:n.835G>C
ENST00000638975.1:c.197G>C ENSP00000492630.1:p.Ser66Thr
ENST00000639431.1:c.265+107763G>C ENSP00000491057.1:n.265+107763G>C
XM_011543675.1:c.13565G>C XP_011541977.1:p.Ser4522Thr
XM_011543676.1:c.13487G>C XP_011541978.1:p.Ser4496Thr
XM_011543677.1:c.10871G>C XP_011541979.1:p.Ser3624Thr
XM_011543678.1:c.13568G>C XP_011541980.1:p.Ser4523Thr
XM_017009963.2:c.13589G>C XP_016865452.1:p.Ser4530Thr
XM_017009964.2:c.13586G>C XP_016865453.1:p.Ser4529Thr
XM_017009965.1:c.13586G>C XP_016865454.1:p.Ser4529Thr
XM_017009966.2:c.13508G>C XP_016865455.1:p.Ser4503Thr
XM_017009967.1:c.13493G>C XP_016865456.1:p.Ser4498Thr
XM_017009968.2:c.13589G>C XP_016865457.1:p.Ser4530Thr
XM_017009969.2:c.13589G>C XP_016865458.1:p.Ser4530Thr
XM_017009970.2:c.13589G>C XP_016865459.1:p.Ser4530Thr
XM_017009971.2:c.13589G>C XP_016865460.1:p.Ser4530Thr
XM_017009972.1:c.6707G>C XP_016865461.1:p.Ser2236Thr
XM_017009973.1:c.6686G>C XP_016865462.1:p.Ser2229Thr