Canonical Allele Identifier: CA360409717

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106561A>C (hg19) ; chr5:g.90810744A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810744A>C , CM000667.2:g.90810744A>C	GRCh38
NC_000005.9:g.90106561A>C , CM000667.1:g.90106561A>C	GRCh37
NC_000005.8:g.90142317A>C	NCBI36
NG_007083.1:g.256945A>C
NG_007083.2:g.286401A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.15484A>C MANE Select	ENSP00000384582.2:p.Ser5162Arg
ENST00000425867.3:c.4438A>C	ENSP00000392618.3:p.Ser1480Arg
ENST00000638510.1:n.2751A>C
ENST00000639431.1:c.265+134535A>C	ENSP00000491057.1:n.265+134535A>C
ENST00000640407.1:c.1894A>C	ENSP00000491425.1:p.Ser632Arg
ENST00000405460.6:c.15484A>C	ENSP00000384582.2:p.Ser5162Arg
ENST00000425867.2:c.2467A>C	ENSP00000392618.2:p.Ser823Arg
NM_032119.3:c.15484A>C	NP_115495.3:p.Ser5162Arg
NR_003149.1:n.15497A>C
XM_011543675.1:c.15481A>C	XP_011541977.1:p.Ser5161Arg
XM_011543676.1:c.15403A>C	XP_011541978.1:p.Ser5135Arg
XM_011543677.1:c.12787A>C	XP_011541979.1:p.Ser4263Arg
NM_032119.4:c.15484A>C MANE Select	NP_115495.3:p.Ser5162Arg
XM_017009963.2:c.15505A>C	XP_016865452.1:p.Ser5169Arg
XM_017009964.2:c.15502A>C	XP_016865453.1:p.Ser5168Arg
XM_017009965.1:c.15502A>C	XP_016865454.1:p.Ser5168Arg
XM_017009966.2:c.15424A>C	XP_016865455.1:p.Ser5142Arg
XM_017009967.1:c.15409A>C	XP_016865456.1:p.Ser5137Arg
XM_017009968.2:c.15325A>C	XP_016865457.1:p.Ser5109Arg
XM_017009969.2:c.15505A>C	XP_016865458.1:p.Ser5169Arg
XM_017009971.2:c.*438A>C	XP_016865460.1:n.*438A>C
XM_017009972.1:c.8623A>C	XP_016865461.1:p.Ser2875Arg
XM_017009973.1:c.8602A>C	XP_016865462.1:p.Ser2868Arg
NR_003149.2:n.15500A>C