Canonical Allele Identifier: CA3338751
Community Standard Title: NM_032119.4(ADGRV1):c.1801G>T (p.Asp601Tyr)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90629501G>T , CM000667.2:g.90629501G>T GRCh38
NC_000005.9:g.89925318G>T , CM000667.1:g.89925318G>T GRCh37
NC_000005.8:g.89961074G>T NCBI36
NG_007083.1:g.75702G>T
NG_007083.2:g.105158G>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.1801G>T MANE Select NP_115495.3:p.Asp601Tyr
ENST00000405460.9:c.1801G>T MANE Select ENSP00000384582.2:p.Asp601Tyr
NM_032119.3:c.1801G>T NP_115495.3:p.Asp601Tyr
NR_003149.1:n.1897G>T
NR_003149.2:n.1900G>T
ENST00000405460.6:c.1801G>T ENSP00000384582.2:p.Asp601Tyr
ENST00000504142.1:c.566G>T
ENST00000504142.2:n.567G>T
ENST00000640109.1:n.1897G>T
XM_011543675.1:c.1801G>T XP_011541977.1:p.Asp601Tyr
XM_011543676.1:c.1801G>T XP_011541978.1:p.Asp601Tyr
XM_011543678.1:c.1801G>T XP_011541980.1:p.Asp601Tyr
XM_011543679.1:c.1801G>T XP_011541981.1:p.Asp601Tyr
XM_017009963.2:c.1801G>T XP_016865452.1:p.Asp601Tyr
XM_017009964.2:c.1801G>T XP_016865453.1:p.Asp601Tyr
XM_017009965.1:c.1798G>T XP_016865454.1:p.Asp600Tyr
XM_017009966.2:c.1801G>T XP_016865455.1:p.Asp601Tyr
XM_017009967.1:c.1705G>T XP_016865456.1:p.Asp569Tyr
XM_017009968.2:c.1801G>T XP_016865457.1:p.Asp601Tyr
XM_017009969.2:c.1801G>T XP_016865458.1:p.Asp601Tyr
XM_017009970.2:c.1801G>T XP_016865459.1:p.Asp601Tyr
XM_017009971.2:c.1801G>T XP_016865460.1:p.Asp601Tyr
XM_017009974.2:c.1801G>T XP_016865463.1:p.Asp601Tyr