Canonical Allele Identifier: CA360425440

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119243G>C (hg19) ; chr5:g.90823426G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823426G>C , CM000667.2:g.90823426G>C	GRCh38
NC_000005.9:g.90119243G>C , CM000667.1:g.90119243G>C	GRCh37
NC_000005.8:g.90154999G>C	NCBI36
NG_007083.1:g.269627G>C
NG_007083.2:g.299083G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16198G>C MANE Select	ENSP00000384582.2:p.Ala5400Pro
ENST00000425867.3:c.5152G>C	ENSP00000392618.3:p.Ala1718Pro
ENST00000638510.1:n.3465G>C
ENST00000639431.1:c.265+147217G>C	ENSP00000491057.1:n.265+147217G>C
ENST00000640061.1:n.128+1244G>C
ENST00000640407.1:c.2608G>C	ENSP00000491425.1:p.Ala870Pro
ENST00000405460.6:c.16198G>C	ENSP00000384582.2:p.Ala5400Pro
ENST00000425867.2:c.3181G>C	ENSP00000392618.2:p.Ala1061Pro
NM_032119.3:c.16198G>C	NP_115495.3:p.Ala5400Pro
NR_003149.1:n.16211G>C
XM_011543675.1:c.16195G>C	XP_011541977.1:p.Ala5399Pro
XM_011543676.1:c.16117G>C	XP_011541978.1:p.Ala5373Pro
XM_011543677.1:c.13501G>C	XP_011541979.1:p.Ala4501Pro
NM_032119.4:c.16198G>C MANE Select	NP_115495.3:p.Ala5400Pro
XM_017009963.2:c.16219G>C	XP_016865452.1:p.Ala5407Pro
XM_017009964.2:c.16216G>C	XP_016865453.1:p.Ala5406Pro
XM_017009965.1:c.16216G>C	XP_016865454.1:p.Ala5406Pro
XM_017009966.2:c.16138G>C	XP_016865455.1:p.Ala5380Pro
XM_017009967.1:c.16123G>C	XP_016865456.1:p.Ala5375Pro
XM_017009968.2:c.16039G>C	XP_016865457.1:p.Ala5347Pro
XM_017009969.2:c.16219G>C	XP_016865458.1:p.Ala5407Pro
XM_017009972.1:c.9337G>C	XP_016865461.1:p.Ala3113Pro
XM_017009973.1:c.9316G>C	XP_016865462.1:p.Ala3106Pro
NR_003149.2:n.16214G>C