Canonical Allele Identifier: CA360410366

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106721C>A (hg19) ; chr5:g.90810904C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810904C>A , CM000667.2:g.90810904C>A	GRCh38
NC_000005.9:g.90106721C>A , CM000667.1:g.90106721C>A	GRCh37
NC_000005.8:g.90142477C>A	NCBI36
NG_007083.1:g.257105C>A
NG_007083.2:g.286561C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15644C>A MANE Select	ENSP00000384582.2:p.Ser5215Tyr
ENST00000425867.3:c.4598C>A	ENSP00000392618.3:p.Ser1533Tyr
ENST00000638510.1:n.2911C>A
ENST00000639431.1:c.265+134695C>A	ENSP00000491057.1:n.265+134695C>A
ENST00000640407.1:c.2054C>A	ENSP00000491425.1:p.Ser685Tyr
ENST00000405460.6:c.15644C>A	ENSP00000384582.2:p.Ser5215Tyr
ENST00000425867.2:c.2627C>A	ENSP00000392618.2:p.Ser876Tyr
NM_032119.3:c.15644C>A	NP_115495.3:p.Ser5215Tyr
NR_003149.1:n.15657C>A
XM_011543675.1:c.15641C>A	XP_011541977.1:p.Ser5214Tyr
XM_011543676.1:c.15563C>A	XP_011541978.1:p.Ser5188Tyr
XM_011543677.1:c.12947C>A	XP_011541979.1:p.Ser4316Tyr
NM_032119.4:c.15644C>A MANE Select	NP_115495.3:p.Ser5215Tyr
XM_017009963.2:c.15665C>A	XP_016865452.1:p.Ser5222Tyr
XM_017009964.2:c.15662C>A	XP_016865453.1:p.Ser5221Tyr
XM_017009965.1:c.15662C>A	XP_016865454.1:p.Ser5221Tyr
XM_017009966.2:c.15584C>A	XP_016865455.1:p.Ser5195Tyr
XM_017009967.1:c.15569C>A	XP_016865456.1:p.Ser5190Tyr
XM_017009968.2:c.15485C>A	XP_016865457.1:p.Ser5162Tyr
XM_017009969.2:c.15665C>A	XP_016865458.1:p.Ser5222Tyr
XM_017009972.1:c.8783C>A	XP_016865461.1:p.Ser2928Tyr
XM_017009973.1:c.8762C>A	XP_016865462.1:p.Ser2921Tyr
NR_003149.2:n.15660C>A