Canonical Allele Identifier: CA445468279

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106821T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811004T>C , CM000667.2:g.90811004T>C	GRCh38
NC_000005.9:g.90106821T>C , CM000667.1:g.90106821T>C	GRCh37
NC_000005.8:g.90142577T>C	NCBI36
NG_007083.1:g.257205T>C
NG_007083.2:g.286661T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15744T>C MANE Select	ENSP00000384582.2:p.Thr5248=
ENST00000425867.3:c.4698T>C	ENSP00000392618.3:p.Thr1566=
ENST00000638510.1:n.3011T>C
ENST00000639431.1:c.265+134795T>C	ENSP00000491057.1:n.265+134795T>C
ENST00000640407.1:c.2154T>C	ENSP00000491425.1:p.Thr718=
ENST00000405460.6:c.15744T>C	ENSP00000384582.2:p.Thr5248=
ENST00000425867.2:c.2727T>C	ENSP00000392618.2:p.Thr909=
NM_032119.3:c.15744T>C	NP_115495.3:p.Thr5248=
NR_003149.1:n.15757T>C
XM_011543675.1:c.15741T>C	XP_011541977.1:p.Thr5247=
XM_011543676.1:c.15663T>C	XP_011541978.1:p.Thr5221=
XM_011543677.1:c.13047T>C	XP_011541979.1:p.Thr4349=
NM_032119.4:c.15744T>C MANE Select	NP_115495.3:p.Thr5248=
XM_017009963.2:c.15765T>C	XP_016865452.1:p.Thr5255=
XM_017009964.2:c.15762T>C	XP_016865453.1:p.Thr5254=
XM_017009965.1:c.15762T>C	XP_016865454.1:p.Thr5254=
XM_017009966.2:c.15684T>C	XP_016865455.1:p.Thr5228=
XM_017009967.1:c.15669T>C	XP_016865456.1:p.Thr5223=
XM_017009968.2:c.15585T>C	XP_016865457.1:p.Thr5195=
XM_017009969.2:c.15765T>C	XP_016865458.1:p.Thr5255=
XM_017009972.1:c.8883T>C	XP_016865461.1:p.Thr2961=
XM_017009973.1:c.8862T>C	XP_016865462.1:p.Thr2954=
NR_003149.2:n.15760T>C