Canonical Allele Identifier: CA360425561

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119304A>C (hg19) ; chr5:g.90823487A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823487A>C , CM000667.2:g.90823487A>C	GRCh38
NC_000005.9:g.90119304A>C , CM000667.1:g.90119304A>C	GRCh37
NC_000005.8:g.90155060A>C	NCBI36
NG_007083.1:g.269688A>C
NG_007083.2:g.299144A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.16259A>C MANE Select	ENSP00000384582.2:p.Gln5420Pro
ENST00000425867.3:c.5213A>C	ENSP00000392618.3:p.Gln1738Pro
ENST00000638510.1:n.3526A>C
ENST00000639431.1:c.265+147278A>C	ENSP00000491057.1:n.265+147278A>C
ENST00000640061.1:n.128+1305A>C
ENST00000640407.1:c.2669A>C	ENSP00000491425.1:p.Gln890Pro
ENST00000405460.6:c.16259A>C	ENSP00000384582.2:p.Gln5420Pro
ENST00000425867.2:c.3242A>C	ENSP00000392618.2:p.Gln1081Pro
NM_032119.3:c.16259A>C	NP_115495.3:p.Gln5420Pro
NR_003149.1:n.16272A>C
XM_011543675.1:c.16256A>C	XP_011541977.1:p.Gln5419Pro
XM_011543676.1:c.16178A>C	XP_011541978.1:p.Gln5393Pro
XM_011543677.1:c.13562A>C	XP_011541979.1:p.Gln4521Pro
NM_032119.4:c.16259A>C MANE Select	NP_115495.3:p.Gln5420Pro
XM_017009963.2:c.16280A>C	XP_016865452.1:p.Gln5427Pro
XM_017009964.2:c.16277A>C	XP_016865453.1:p.Gln5426Pro
XM_017009965.1:c.16277A>C	XP_016865454.1:p.Gln5426Pro
XM_017009966.2:c.16199A>C	XP_016865455.1:p.Gln5400Pro
XM_017009967.1:c.16184A>C	XP_016865456.1:p.Gln5395Pro
XM_017009968.2:c.16100A>C	XP_016865457.1:p.Gln5367Pro
XM_017009969.2:c.16280A>C	XP_016865458.1:p.Gln5427Pro
XM_017009972.1:c.9398A>C	XP_016865461.1:p.Gln3133Pro
XM_017009973.1:c.9377A>C	XP_016865462.1:p.Gln3126Pro
NR_003149.2:n.16275A>C