Canonical Allele Identifier: CA360410700

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106818A>C (hg19) ; chr5:g.90811001A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811001A>C , CM000667.2:g.90811001A>C	GRCh38
NC_000005.9:g.90106818A>C , CM000667.1:g.90106818A>C	GRCh37
NC_000005.8:g.90142574A>C	NCBI36
NG_007083.1:g.257202A>C
NG_007083.2:g.286658A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.15741A>C MANE Select	ENSP00000384582.2:p.Arg5247Ser
ENST00000425867.3:c.4695A>C	ENSP00000392618.3:p.Arg1565Ser
ENST00000638510.1:n.3008A>C
ENST00000639431.1:c.265+134792A>C	ENSP00000491057.1:n.265+134792A>C
ENST00000640407.1:c.2151A>C	ENSP00000491425.1:p.Arg717Ser
ENST00000405460.6:c.15741A>C	ENSP00000384582.2:p.Arg5247Ser
ENST00000425867.2:c.2724A>C	ENSP00000392618.2:p.Arg908Ser
NM_032119.3:c.15741A>C	NP_115495.3:p.Arg5247Ser
NR_003149.1:n.15754A>C
XM_011543675.1:c.15738A>C	XP_011541977.1:p.Arg5246Ser
XM_011543676.1:c.15660A>C	XP_011541978.1:p.Arg5220Ser
XM_011543677.1:c.13044A>C	XP_011541979.1:p.Arg4348Ser
NM_032119.4:c.15741A>C MANE Select	NP_115495.3:p.Arg5247Ser
XM_017009963.2:c.15762A>C	XP_016865452.1:p.Arg5254Ser
XM_017009964.2:c.15759A>C	XP_016865453.1:p.Arg5253Ser
XM_017009965.1:c.15759A>C	XP_016865454.1:p.Arg5253Ser
XM_017009966.2:c.15681A>C	XP_016865455.1:p.Arg5227Ser
XM_017009967.1:c.15666A>C	XP_016865456.1:p.Arg5222Ser
XM_017009968.2:c.15582A>C	XP_016865457.1:p.Arg5194Ser
XM_017009969.2:c.15762A>C	XP_016865458.1:p.Arg5254Ser
XM_017009972.1:c.8880A>C	XP_016865461.1:p.Arg2960Ser
XM_017009973.1:c.8859A>C	XP_016865462.1:p.Arg2953Ser
NR_003149.2:n.15757A>C