Canonical Allele Identifier: CA445467994

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106725T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810908T>C , CM000667.2:g.90810908T>C	GRCh38
NC_000005.9:g.90106725T>C , CM000667.1:g.90106725T>C	GRCh37
NC_000005.8:g.90142481T>C	NCBI36
NG_007083.1:g.257109T>C
NG_007083.2:g.286565T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15648T>C MANE Select	ENSP00000384582.2:p.Ile5216=
ENST00000425867.3:c.4602T>C	ENSP00000392618.3:p.Ile1534=
ENST00000638510.1:n.2915T>C
ENST00000639431.1:c.265+134699T>C	ENSP00000491057.1:n.265+134699T>C
ENST00000640407.1:c.2058T>C	ENSP00000491425.1:p.Ile686=
ENST00000405460.6:c.15648T>C	ENSP00000384582.2:p.Ile5216=
ENST00000425867.2:c.2631T>C	ENSP00000392618.2:p.Ile877=
NM_032119.3:c.15648T>C	NP_115495.3:p.Ile5216=
NR_003149.1:n.15661T>C
XM_011543675.1:c.15645T>C	XP_011541977.1:p.Ile5215=
XM_011543676.1:c.15567T>C	XP_011541978.1:p.Ile5189=
XM_011543677.1:c.12951T>C	XP_011541979.1:p.Ile4317=
NM_032119.4:c.15648T>C MANE Select	NP_115495.3:p.Ile5216=
XM_017009963.2:c.15669T>C	XP_016865452.1:p.Ile5223=
XM_017009964.2:c.15666T>C	XP_016865453.1:p.Ile5222=
XM_017009965.1:c.15666T>C	XP_016865454.1:p.Ile5222=
XM_017009966.2:c.15588T>C	XP_016865455.1:p.Ile5196=
XM_017009967.1:c.15573T>C	XP_016865456.1:p.Ile5191=
XM_017009968.2:c.15489T>C	XP_016865457.1:p.Ile5163=
XM_017009969.2:c.15669T>C	XP_016865458.1:p.Ile5223=
XM_017009972.1:c.8787T>C	XP_016865461.1:p.Ile2929=
XM_017009973.1:c.8766T>C	XP_016865462.1:p.Ile2922=
NR_003149.2:n.15664T>C