Canonical Allele Identifier: CA360410704

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106819A>C (hg19) ; chr5:g.90811002A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811002A>C , CM000667.2:g.90811002A>C	GRCh38
NC_000005.9:g.90106819A>C , CM000667.1:g.90106819A>C	GRCh37
NC_000005.8:g.90142575A>C	NCBI36
NG_007083.1:g.257203A>C
NG_007083.2:g.286659A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15742A>C MANE Select	ENSP00000384582.2:p.Thr5248Pro
ENST00000425867.3:c.4696A>C	ENSP00000392618.3:p.Thr1566Pro
ENST00000638510.1:n.3009A>C
ENST00000639431.1:c.265+134793A>C	ENSP00000491057.1:n.265+134793A>C
ENST00000640407.1:c.2152A>C	ENSP00000491425.1:p.Thr718Pro
ENST00000405460.6:c.15742A>C	ENSP00000384582.2:p.Thr5248Pro
ENST00000425867.2:c.2725A>C	ENSP00000392618.2:p.Thr909Pro
NM_032119.3:c.15742A>C	NP_115495.3:p.Thr5248Pro
NR_003149.1:n.15755A>C
XM_011543675.1:c.15739A>C	XP_011541977.1:p.Thr5247Pro
XM_011543676.1:c.15661A>C	XP_011541978.1:p.Thr5221Pro
XM_011543677.1:c.13045A>C	XP_011541979.1:p.Thr4349Pro
NM_032119.4:c.15742A>C MANE Select	NP_115495.3:p.Thr5248Pro
XM_017009963.2:c.15763A>C	XP_016865452.1:p.Thr5255Pro
XM_017009964.2:c.15760A>C	XP_016865453.1:p.Thr5254Pro
XM_017009965.1:c.15760A>C	XP_016865454.1:p.Thr5254Pro
XM_017009966.2:c.15682A>C	XP_016865455.1:p.Thr5228Pro
XM_017009967.1:c.15667A>C	XP_016865456.1:p.Thr5223Pro
XM_017009968.2:c.15583A>C	XP_016865457.1:p.Thr5195Pro
XM_017009969.2:c.15763A>C	XP_016865458.1:p.Thr5255Pro
XM_017009972.1:c.8881A>C	XP_016865461.1:p.Thr2961Pro
XM_017009973.1:c.8860A>C	XP_016865462.1:p.Thr2954Pro
NR_003149.2:n.15758A>C