Canonical Allele Identifier: CA445467961

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106713C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810896C>T , CM000667.2:g.90810896C>T	GRCh38
NC_000005.9:g.90106713C>T , CM000667.1:g.90106713C>T	GRCh37
NC_000005.8:g.90142469C>T	NCBI36
NG_007083.1:g.257097C>T
NG_007083.2:g.286553C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15636C>T MANE Select	ENSP00000384582.2:p.Ala5212=
ENST00000425867.3:c.4590C>T	ENSP00000392618.3:p.Ala1530=
ENST00000638510.1:n.2903C>T
ENST00000639431.1:c.265+134687C>T	ENSP00000491057.1:n.265+134687C>T
ENST00000640407.1:c.2046C>T	ENSP00000491425.1:p.Ala682=
ENST00000405460.6:c.15636C>T	ENSP00000384582.2:p.Ala5212=
ENST00000425867.2:c.2619C>T	ENSP00000392618.2:p.Ala873=
NM_032119.3:c.15636C>T	NP_115495.3:p.Ala5212=
NR_003149.1:n.15649C>T
XM_011543675.1:c.15633C>T	XP_011541977.1:p.Ala5211=
XM_011543676.1:c.15555C>T	XP_011541978.1:p.Ala5185=
XM_011543677.1:c.12939C>T	XP_011541979.1:p.Ala4313=
NM_032119.4:c.15636C>T MANE Select	NP_115495.3:p.Ala5212=
XM_017009963.2:c.15657C>T	XP_016865452.1:p.Ala5219=
XM_017009964.2:c.15654C>T	XP_016865453.1:p.Ala5218=
XM_017009965.1:c.15654C>T	XP_016865454.1:p.Ala5218=
XM_017009966.2:c.15576C>T	XP_016865455.1:p.Ala5192=
XM_017009967.1:c.15561C>T	XP_016865456.1:p.Ala5187=
XM_017009968.2:c.15477C>T	XP_016865457.1:p.Ala5159=
XM_017009969.2:c.15657C>T	XP_016865458.1:p.Ala5219=
XM_017009972.1:c.8775C>T	XP_016865461.1:p.Ala2925=
XM_017009973.1:c.8754C>T	XP_016865462.1:p.Ala2918=
NR_003149.2:n.15652C>T