Canonical Allele Identifier: CA360401227

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086916A>C (hg19) ; chr5:g.90791099A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791099A>C , CM000667.2:g.90791099A>C	GRCh38
NC_000005.9:g.90086916A>C , CM000667.1:g.90086916A>C	GRCh37
NC_000005.8:g.90122672A>C	NCBI36
NG_007083.1:g.237300A>C
NG_007083.2:g.266756A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14270A>C MANE Select	ENSP00000384582.2:p.Asn4757Thr
ENST00000425867.3:c.3224A>C	ENSP00000392618.3:p.Asn1075Thr
ENST00000638510.1:n.1537A>C
ENST00000638585.1:n.36A>C
ENST00000638975.1:c.899A>C	ENSP00000492630.1:p.Asn300Thr
ENST00000639431.1:c.265+114890A>C	ENSP00000491057.1:n.265+114890A>C
ENST00000640407.1:c.680A>C	ENSP00000491425.1:p.Asn227Thr
ENST00000405460.6:c.14270A>C	ENSP00000384582.2:p.Asn4757Thr
ENST00000425867.2:c.1253A>C	ENSP00000392618.2:p.Asn418Thr
NM_032119.3:c.14270A>C	NP_115495.3:p.Asn4757Thr
NR_003149.1:n.14283A>C
XM_011543675.1:c.14267A>C	XP_011541977.1:p.Asn4756Thr
XM_011543676.1:c.14189A>C	XP_011541978.1:p.Asn4730Thr
XM_011543677.1:c.11573A>C	XP_011541979.1:p.Asn3858Thr
XM_011543678.1:c.14270A>C	XP_011541980.1:p.Asn4757Thr
NM_032119.4:c.14270A>C MANE Select	NP_115495.3:p.Asn4757Thr
XM_017009963.2:c.14291A>C	XP_016865452.1:p.Asn4764Thr
XM_017009964.2:c.14288A>C	XP_016865453.1:p.Asn4763Thr
XM_017009965.1:c.14288A>C	XP_016865454.1:p.Asn4763Thr
XM_017009966.2:c.14210A>C	XP_016865455.1:p.Asn4737Thr
XM_017009967.1:c.14195A>C	XP_016865456.1:p.Asn4732Thr
XM_017009968.2:c.14291A>C	XP_016865457.1:p.Asn4764Thr
XM_017009969.2:c.14291A>C	XP_016865458.1:p.Asn4764Thr
XM_017009970.2:c.14291A>C	XP_016865459.1:p.Asn4764Thr
XM_017009971.2:c.14291A>C	XP_016865460.1:p.Asn4764Thr
XM_017009972.1:c.7409A>C	XP_016865461.1:p.Asn2470Thr
XM_017009973.1:c.7388A>C	XP_016865462.1:p.Asn2463Thr
NR_003149.2:n.14286A>C