Canonical Allele Identifier: CA1562910056

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90807650G= , CM000667.2:g.90807650G=	GRCh38
NC_000005.9:g.90103467G= , CM000667.1:g.90103467G=	GRCh37
NC_000005.8:g.90139223G=	NCBI36
NG_007083.1:g.253851G=
NG_007083.2:g.283307G=

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14885G= MANE Select	NP_115495.3:p.Trp4962=
ENST00000405460.9:c.14885G= MANE Select	ENSP00000384582.2:p.Trp4962=
NM_032119.3:c.14885G=	NP_115495.3:p.Trp4962=
NR_003149.1:n.14898G=
NR_003149.2:n.14901G=
ENST00000405460.6:c.14885G=	ENSP00000384582.2:p.Trp4962=
ENST00000425867.2:c.1868G=	ENSP00000392618.2:p.Trp623=
ENST00000425867.3:c.3839G=	ENSP00000392618.3:p.Trp1280=
ENST00000513828.1:n.581G=
ENST00000638510.1:n.2152G=
ENST00000638585.1:n.428-2583G=
ENST00000639431.1:c.265+131441G=	ENSP00000491057.1:n.265+131441G=
ENST00000640407.1:c.1295G=	ENSP00000491425.1:p.Trp432=
XM_011543675.1:c.14882G=	XP_011541977.1:p.Trp4961=
XM_011543676.1:c.14804G=	XP_011541978.1:p.Trp4935=
XM_011543677.1:c.12188G=	XP_011541979.1:p.Trp4063=
XM_011543678.1:c.14885G=	XP_011541980.1:p.Trp4962=
XM_017009963.2:c.14906G=	XP_016865452.1:p.Trp4969=
XM_017009964.2:c.14903G=	XP_016865453.1:p.Trp4968=
XM_017009965.1:c.14903G=	XP_016865454.1:p.Trp4968=
XM_017009966.2:c.14825G=	XP_016865455.1:p.Trp4942=
XM_017009967.1:c.14810G=	XP_016865456.1:p.Trp4937=
XM_017009968.2:c.14731G=	XP_016865457.1:p.Gly4911=
XM_017009969.2:c.14906G=	XP_016865458.1:p.Trp4969=
XM_017009970.2:c.14906G=	XP_016865459.1:p.Trp4969=
XM_017009971.2:c.14731G=	XP_016865460.1:p.Gly4911=
XM_017009972.1:c.8024G=	XP_016865461.1:p.Trp2675=
XM_017009973.1:c.8003G=	XP_016865462.1:p.Trp2668=