Canonical Allele Identifier: CA360377312

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059153A>C (hg19) ; chr5:g.90763336A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763336A>C , CM000667.2:g.90763336A>C	GRCh38
NC_000005.9:g.90059153A>C , CM000667.1:g.90059153A>C	GRCh37
NC_000005.8:g.90094909A>C	NCBI36
NG_007083.1:g.209537A>C
NG_007083.2:g.238993A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12152A>C MANE Select	ENSP00000384582.2:p.Asp4051Ala
ENST00000425867.3:c.1106A>C	ENSP00000392618.3:p.Asp369Ala
ENST00000639431.1:c.265+87127A>C	ENSP00000491057.1:n.265+87127A>C
ENST00000640464.1:n.2571A>C
ENST00000640729.1:n.729A>C
ENST00000405460.6:c.12152A>C	ENSP00000384582.2:p.Asp4051Ala
NM_032119.3:c.12152A>C	NP_115495.3:p.Asp4051Ala
NR_003149.1:n.12165A>C
XM_011543675.1:c.12149A>C	XP_011541977.1:p.Asp4050Ala
XM_011543676.1:c.12071A>C	XP_011541978.1:p.Asp4024Ala
XM_011543677.1:c.9455A>C	XP_011541979.1:p.Asp3152Ala
XM_011543678.1:c.12152A>C	XP_011541980.1:p.Asp4051Ala
NM_032119.4:c.12152A>C MANE Select	NP_115495.3:p.Asp4051Ala
XM_017009963.2:c.12173A>C	XP_016865452.1:p.Asp4058Ala
XM_017009964.2:c.12170A>C	XP_016865453.1:p.Asp4057Ala
XM_017009965.1:c.12170A>C	XP_016865454.1:p.Asp4057Ala
XM_017009966.2:c.12092A>C	XP_016865455.1:p.Asp4031Ala
XM_017009967.1:c.12077A>C	XP_016865456.1:p.Asp4026Ala
XM_017009968.2:c.12173A>C	XP_016865457.1:p.Asp4058Ala
XM_017009969.2:c.12173A>C	XP_016865458.1:p.Asp4058Ala
XM_017009970.2:c.12173A>C	XP_016865459.1:p.Asp4058Ala
XM_017009971.2:c.12173A>C	XP_016865460.1:p.Asp4058Ala
XM_017009972.1:c.5291A>C	XP_016865461.1:p.Asp1764Ala
XM_017009973.1:c.5270A>C	XP_016865462.1:p.Asp1757Ala
NR_003149.2:n.12168A>C