Canonical Allele Identifier: CA3340803
Community Standard Title: NM_032119.4(ADGRV1):c.10648G>T (p.Asp3550Tyr)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90745144G>T , CM000667.2:g.90745144G>T GRCh38
NC_000005.9:g.90040961G>T , CM000667.1:g.90040961G>T GRCh37
NC_000005.8:g.90076717G>T NCBI36
NG_007083.1:g.191345G>T
NG_007083.2:g.220801G>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.10648G>T MANE Select NP_115495.3:p.Asp3550Tyr
ENST00000405460.9:c.10648G>T MANE Select ENSP00000384582.2:p.Asp3550Tyr
NM_032119.3:c.10648G>T NP_115495.3:p.Asp3550Tyr
NR_003149.1:n.10661G>T
NR_003149.2:n.10664G>T
ENST00000405460.6:c.10648G>T ENSP00000384582.2:p.Asp3550Tyr
ENST00000509621.1:c.3345G>T
ENST00000639431.1:c.265+68935G>T ENSP00000491057.1:n.265+68935G>T
ENST00000640374.1:n.3792G>T
ENST00000640464.1:n.1067G>T
XM_011543675.1:c.10645G>T XP_011541977.1:p.Asp3549Tyr
XM_011543676.1:c.10567G>T XP_011541978.1:p.Asp3523Tyr
XM_011543677.1:c.7951G>T XP_011541979.1:p.Asp2651Tyr
XM_011543678.1:c.10648G>T XP_011541980.1:p.Asp3550Tyr
XM_011543679.1:c.10648G>T XP_011541981.1:p.Asp3550Tyr
XM_017009963.2:c.10669G>T XP_016865452.1:p.Asp3557Tyr
XM_017009964.2:c.10666G>T XP_016865453.1:p.Asp3556Tyr
XM_017009965.1:c.10666G>T XP_016865454.1:p.Asp3556Tyr
XM_017009966.2:c.10588G>T XP_016865455.1:p.Asp3530Tyr
XM_017009967.1:c.10573G>T XP_016865456.1:p.Asp3525Tyr
XM_017009968.2:c.10669G>T XP_016865457.1:p.Asp3557Tyr
XM_017009969.2:c.10669G>T XP_016865458.1:p.Asp3557Tyr
XM_017009970.2:c.10669G>T XP_016865459.1:p.Asp3557Tyr
XM_017009971.2:c.10669G>T XP_016865460.1:p.Asp3557Tyr
XM_017009972.1:c.3787G>T XP_016865461.1:p.Asp1263Tyr
XM_017009973.1:c.3766G>T XP_016865462.1:p.Asp1256Tyr
XM_017009974.2:c.10669G>T XP_016865463.1:p.Asp3557Tyr