Canonical Allele Identifier: CA360426887

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90261317A>C (hg19) ; chr5:g.90965500A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90965500A>C , CM000667.2:g.90965500A>C	GRCh38
NC_000005.9:g.90261317A>C , CM000667.1:g.90261317A>C	GRCh37
NC_000005.8:g.90297073A>C	NCBI36
NG_007083.1:g.411701A>C
NG_007083.2:g.441157A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.17942A>C MANE Select	ENSP00000384582.2:p.Tyr5981Ser
ENST00000425867.3:c.6896A>C	ENSP00000392618.3:p.Tyr2299Ser
ENST00000638510.1:n.5209A>C
ENST00000638990.1:c.1154A>C
ENST00000639431.1:c.266-19844A>C	ENSP00000491057.1:n.266-19844A>C
ENST00000639707.1:c.26A>C	ENSP00000492328.1:p.Tyr9Ser
ENST00000639821.1:c.26A>C	ENSP00000492216.1:p.Tyr9Ser
ENST00000640369.1:c.26A>C	ENSP00000491401.1:p.Tyr9Ser
ENST00000640407.1:c.4391A>C	ENSP00000491425.1:n.4391A>C
ENST00000640815.1:c.26A>C	ENSP00000491767.1:p.Tyr9Ser
ENST00000405460.6:c.17942A>C	ENSP00000384582.2:p.Tyr5981Ser
ENST00000425867.2:c.4925A>C	ENSP00000392618.2:p.Tyr1642Ser
NM_032119.3:c.17942A>C	NP_115495.3:p.Tyr5981Ser
NR_003149.1:n.17955A>C
XM_011543675.1:c.17939A>C	XP_011541977.1:p.Tyr5980Ser
XM_011543676.1:c.17861A>C	XP_011541978.1:p.Tyr5954Ser
XM_011543677.1:c.15245A>C	XP_011541979.1:p.Tyr5082Ser
NM_032119.4:c.17942A>C MANE Select	NP_115495.3:p.Tyr5981Ser
XM_017009963.2:c.17963A>C	XP_016865452.1:p.Tyr5988Ser
XM_017009964.2:c.17960A>C	XP_016865453.1:p.Tyr5987Ser
XM_017009965.1:c.17960A>C	XP_016865454.1:p.Tyr5987Ser
XM_017009966.2:c.17882A>C	XP_016865455.1:p.Tyr5961Ser
XM_017009967.1:c.17867A>C	XP_016865456.1:p.Tyr5956Ser
XM_017009968.2:c.17783A>C	XP_016865457.1:p.Tyr5928Ser
XM_017009969.2:c.17963A>C	XP_016865458.1:p.Tyr5988Ser
XM_017009972.1:c.11081A>C	XP_016865461.1:p.Tyr3694Ser
XM_017009973.1:c.11060A>C	XP_016865462.1:p.Tyr3687Ser
NR_003149.2:n.17958A>C