Canonical Allele Identifier: CA360367174

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050964A>C (hg19) ; chr5:g.90755147A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755147A>C , CM000667.2:g.90755147A>C	GRCh38
NC_000005.9:g.90050964A>C , CM000667.1:g.90050964A>C	GRCh37
NC_000005.8:g.90086720A>C	NCBI36
NG_007083.1:g.201348A>C
NG_007083.2:g.230804A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11542A>C MANE Select	ENSP00000384582.2:p.Asn3848His
ENST00000425867.3:c.673A>C	ENSP00000392618.3:p.Asn225His
ENST00000639431.1:c.265+78938A>C	ENSP00000491057.1:n.265+78938A>C
ENST00000640374.1:n.4686A>C
ENST00000640464.1:n.1961A>C
ENST00000405460.6:c.11542A>C	ENSP00000384582.2:p.Asn3848His
ENST00000509621.1:c.4239A>C
NM_032119.3:c.11542A>C	NP_115495.3:p.Asn3848His
NR_003149.1:n.11555A>C
XM_011543675.1:c.11539A>C	XP_011541977.1:p.Asn3847His
XM_011543676.1:c.11461A>C	XP_011541978.1:p.Asn3821His
XM_011543677.1:c.8845A>C	XP_011541979.1:p.Asn2949His
XM_011543678.1:c.11542A>C	XP_011541980.1:p.Asn3848His
NM_032119.4:c.11542A>C MANE Select	NP_115495.3:p.Asn3848His
XM_017009963.2:c.11563A>C	XP_016865452.1:p.Asn3855His
XM_017009964.2:c.11560A>C	XP_016865453.1:p.Asn3854His
XM_017009965.1:c.11560A>C	XP_016865454.1:p.Asn3854His
XM_017009966.2:c.11482A>C	XP_016865455.1:p.Asn3828His
XM_017009967.1:c.11467A>C	XP_016865456.1:p.Asn3823His
XM_017009968.2:c.11563A>C	XP_016865457.1:p.Asn3855His
XM_017009969.2:c.11563A>C	XP_016865458.1:p.Asn3855His
XM_017009970.2:c.11563A>C	XP_016865459.1:p.Asn3855His
XM_017009971.2:c.11563A>C	XP_016865460.1:p.Asn3855His
XM_017009972.1:c.4681A>C	XP_016865461.1:p.Asn1561His
XM_017009973.1:c.4660A>C	XP_016865462.1:p.Asn1554His
NR_003149.2:n.11558A>C