Canonical Allele Identifier: CA3341704
Community Standard Title: NM_032119.4(ADGRV1):c.14304G>A (p.Ser4768=)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90791133G>A , CM000667.2:g.90791133G>A GRCh38
NC_000005.9:g.90086950G>A , CM000667.1:g.90086950G>A GRCh37
NC_000005.8:g.90122706G>A NCBI36
NG_007083.1:g.237334G>A
NG_007083.2:g.266790G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.14304G>A MANE Select NP_115495.3:p.Ser4768=
ENST00000405460.9:c.14304G>A MANE Select ENSP00000384582.2:p.Ser4768=
NM_032119.3:c.14304G>A NP_115495.3:p.Ser4768=
NR_003149.1:n.14317G>A
NR_003149.2:n.14320G>A
ENST00000405460.6:c.14304G>A ENSP00000384582.2:p.Ser4768=
ENST00000425867.2:c.1287G>A ENSP00000392618.2:p.Ser429=
ENST00000425867.3:c.3258G>A ENSP00000392618.3:p.Ser1086=
ENST00000638510.1:n.1571G>A
ENST00000638585.1:n.70G>A
ENST00000638975.1:c.933G>A ENSP00000492630.1:p.Ser311=
ENST00000639431.1:c.265+114924G>A ENSP00000491057.1:n.265+114924G>A
ENST00000640407.1:c.714G>A ENSP00000491425.1:p.Ser238=
XM_011543675.1:c.14301G>A XP_011541977.1:p.Ser4767=
XM_011543676.1:c.14223G>A XP_011541978.1:p.Ser4741=
XM_011543677.1:c.11607G>A XP_011541979.1:p.Ser3869=
XM_011543678.1:c.14304G>A XP_011541980.1:p.Ser4768=
XM_017009963.2:c.14325G>A XP_016865452.1:p.Ser4775=
XM_017009964.2:c.14322G>A XP_016865453.1:p.Ser4774=
XM_017009965.1:c.14322G>A XP_016865454.1:p.Ser4774=
XM_017009966.2:c.14244G>A XP_016865455.1:p.Ser4748=
XM_017009967.1:c.14229G>A XP_016865456.1:p.Ser4743=
XM_017009968.2:c.14325G>A XP_016865457.1:p.Ser4775=
XM_017009969.2:c.14325G>A XP_016865458.1:p.Ser4775=
XM_017009970.2:c.14325G>A XP_016865459.1:p.Ser4775=
XM_017009971.2:c.14325G>A XP_016865460.1:p.Ser4775=
XM_017009972.1:c.7443G>A XP_016865461.1:p.Ser2481=
XM_017009973.1:c.7422G>A XP_016865462.1:p.Ser2474=