Canonical Allele Identifier: CA360425656

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119351A>C (hg19) ; chr5:g.90823534A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823534A>C , CM000667.2:g.90823534A>C	GRCh38
NC_000005.9:g.90119351A>C , CM000667.1:g.90119351A>C	GRCh37
NC_000005.8:g.90155107A>C	NCBI36
NG_007083.1:g.269735A>C
NG_007083.2:g.299191A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16306A>C MANE Select	ENSP00000384582.2:p.Thr5436Pro
ENST00000425867.3:c.5260A>C	ENSP00000392618.3:p.Thr1754Pro
ENST00000638510.1:n.3573A>C
ENST00000639431.1:c.265+147325A>C	ENSP00000491057.1:n.265+147325A>C
ENST00000640061.1:n.128+1352A>C
ENST00000640407.1:c.2716A>C	ENSP00000491425.1:p.Thr906Pro
ENST00000405460.6:c.16306A>C	ENSP00000384582.2:p.Thr5436Pro
ENST00000425867.2:c.3289A>C	ENSP00000392618.2:p.Thr1097Pro
NM_032119.3:c.16306A>C	NP_115495.3:p.Thr5436Pro
NR_003149.1:n.16319A>C
XM_011543675.1:c.16303A>C	XP_011541977.1:p.Thr5435Pro
XM_011543676.1:c.16225A>C	XP_011541978.1:p.Thr5409Pro
XM_011543677.1:c.13609A>C	XP_011541979.1:p.Thr4537Pro
NM_032119.4:c.16306A>C MANE Select	NP_115495.3:p.Thr5436Pro
XM_017009963.2:c.16327A>C	XP_016865452.1:p.Thr5443Pro
XM_017009964.2:c.16324A>C	XP_016865453.1:p.Thr5442Pro
XM_017009965.1:c.16324A>C	XP_016865454.1:p.Thr5442Pro
XM_017009966.2:c.16246A>C	XP_016865455.1:p.Thr5416Pro
XM_017009967.1:c.16231A>C	XP_016865456.1:p.Thr5411Pro
XM_017009968.2:c.16147A>C	XP_016865457.1:p.Thr5383Pro
XM_017009969.2:c.16327A>C	XP_016865458.1:p.Thr5443Pro
XM_017009972.1:c.9445A>C	XP_016865461.1:p.Thr3149Pro
XM_017009973.1:c.9424A>C	XP_016865462.1:p.Thr3142Pro
NR_003149.2:n.16322A>C