Canonical Allele Identifier: CA3342016
Community Standard Title: NM_032119.4(ADGRV1):c.15987C>T (p.Tyr5329=)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90811247C>T , CM000667.2:g.90811247C>T GRCh38
NC_000005.9:g.90107064C>T , CM000667.1:g.90107064C>T GRCh37
NC_000005.8:g.90142820C>T NCBI36
NG_007083.1:g.257448C>T
NG_007083.2:g.286904C>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.15987C>T MANE Select NP_115495.3:p.Tyr5329=
ENST00000405460.9:c.15987C>T MANE Select ENSP00000384582.2:p.Tyr5329=
NM_032119.3:c.15987C>T NP_115495.3:p.Tyr5329=
NR_003149.1:n.16000C>T
NR_003149.2:n.16003C>T
ENST00000405460.6:c.15987C>T ENSP00000384582.2:p.Tyr5329=
ENST00000425867.2:c.2970C>T ENSP00000392618.2:p.Tyr990=
ENST00000425867.3:c.4941C>T ENSP00000392618.3:p.Tyr1647=
ENST00000638510.1:n.3254C>T
ENST00000639431.1:c.265+135038C>T ENSP00000491057.1:n.265+135038C>T
ENST00000640407.1:c.2397C>T ENSP00000491425.1:p.Tyr799=
XM_011543675.1:c.15984C>T XP_011541977.1:p.Tyr5328=
XM_011543676.1:c.15906C>T XP_011541978.1:p.Tyr5302=
XM_011543677.1:c.13290C>T XP_011541979.1:p.Tyr4430=
XM_017009963.2:c.16008C>T XP_016865452.1:p.Tyr5336=
XM_017009964.2:c.16005C>T XP_016865453.1:p.Tyr5335=
XM_017009965.1:c.16005C>T XP_016865454.1:p.Tyr5335=
XM_017009966.2:c.15927C>T XP_016865455.1:p.Tyr5309=
XM_017009967.1:c.15912C>T XP_016865456.1:p.Tyr5304=
XM_017009968.2:c.15828C>T XP_016865457.1:p.Tyr5276=
XM_017009969.2:c.16008C>T XP_016865458.1:p.Tyr5336=
XM_017009972.1:c.9126C>T XP_016865461.1:p.Tyr3042=
XM_017009973.1:c.9105C>T XP_016865462.1:p.Tyr3035=