Canonical Allele Identifier: CA445436565

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1184602456
• MyVariant Identifiers: chr5:g.90119320C>T (hg19) ; chr5:g.90823503C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823503C>T , CM000667.2:g.90823503C>T	GRCh38
NC_000005.9:g.90119320C>T , CM000667.1:g.90119320C>T	GRCh37
NC_000005.8:g.90155076C>T	NCBI36
NG_007083.1:g.269704C>T
NG_007083.2:g.299160C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16275C>T MANE Select	ENSP00000384582.2:p.Asn5425=
ENST00000425867.3:c.5229C>T	ENSP00000392618.3:p.Asn1743=
ENST00000638510.1:n.3542C>T
ENST00000639431.1:c.265+147294C>T	ENSP00000491057.1:n.265+147294C>T
ENST00000640061.1:n.128+1321C>T
ENST00000640407.1:c.2685C>T	ENSP00000491425.1:p.Asn895=
ENST00000405460.6:c.16275C>T	ENSP00000384582.2:p.Asn5425=
ENST00000425867.2:c.3258C>T	ENSP00000392618.2:p.Asn1086=
NM_032119.3:c.16275C>T	NP_115495.3:p.Asn5425=
NR_003149.1:n.16288C>T
XM_011543675.1:c.16272C>T	XP_011541977.1:p.Asn5424=
XM_011543676.1:c.16194C>T	XP_011541978.1:p.Asn5398=
XM_011543677.1:c.13578C>T	XP_011541979.1:p.Asn4526=
NM_032119.4:c.16275C>T MANE Select	NP_115495.3:p.Asn5425=
XM_017009963.2:c.16296C>T	XP_016865452.1:p.Asn5432=
XM_017009964.2:c.16293C>T	XP_016865453.1:p.Asn5431=
XM_017009965.1:c.16293C>T	XP_016865454.1:p.Asn5431=
XM_017009966.2:c.16215C>T	XP_016865455.1:p.Asn5405=
XM_017009967.1:c.16200C>T	XP_016865456.1:p.Asn5400=
XM_017009968.2:c.16116C>T	XP_016865457.1:p.Asn5372=
XM_017009969.2:c.16296C>T	XP_016865458.1:p.Asn5432=
XM_017009972.1:c.9414C>T	XP_016865461.1:p.Asn3138=
XM_017009973.1:c.9393C>T	XP_016865462.1:p.Asn3131=
NR_003149.2:n.16291C>T