Canonical Allele Identifier: CA1562908325

Gene: ADGRV1

Genomic Alleles

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

Transcript Alleles

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