Canonical Allele Identifier: CA360401730

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90087033A>C (hg19) ; chr5:g.90791216A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791216A>C , CM000667.2:g.90791216A>C	GRCh38
NC_000005.9:g.90087033A>C , CM000667.1:g.90087033A>C	GRCh37
NC_000005.8:g.90122789A>C	NCBI36
NG_007083.1:g.237417A>C
NG_007083.2:g.266873A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14387A>C MANE Select	ENSP00000384582.2:p.Asp4796Ala
ENST00000425867.3:c.3341A>C	ENSP00000392618.3:p.Asp1114Ala
ENST00000507314.2:c.62A>C	ENSP00000491299.1:p.Asp21Ala
ENST00000638510.1:n.1654A>C
ENST00000638585.1:n.153A>C
ENST00000638975.1:c.1016A>C	ENSP00000492630.1:p.Asp339Ala
ENST00000639431.1:c.265+115007A>C	ENSP00000491057.1:n.265+115007A>C
ENST00000640407.1:c.797A>C	ENSP00000491425.1:p.Asp266Ala
ENST00000405460.6:c.14387A>C	ENSP00000384582.2:p.Asp4796Ala
ENST00000425867.2:c.1370A>C	ENSP00000392618.2:p.Asp457Ala
ENST00000507314.1:n.62A>C
NM_032119.3:c.14387A>C	NP_115495.3:p.Asp4796Ala
NR_003149.1:n.14400A>C
XM_011543675.1:c.14384A>C	XP_011541977.1:p.Asp4795Ala
XM_011543676.1:c.14306A>C	XP_011541978.1:p.Asp4769Ala
XM_011543677.1:c.11690A>C	XP_011541979.1:p.Asp3897Ala
XM_011543678.1:c.14387A>C	XP_011541980.1:p.Asp4796Ala
NM_032119.4:c.14387A>C MANE Select	NP_115495.3:p.Asp4796Ala
XM_017009963.2:c.14408A>C	XP_016865452.1:p.Asp4803Ala
XM_017009964.2:c.14405A>C	XP_016865453.1:p.Asp4802Ala
XM_017009965.1:c.14405A>C	XP_016865454.1:p.Asp4802Ala
XM_017009966.2:c.14327A>C	XP_016865455.1:p.Asp4776Ala
XM_017009967.1:c.14312A>C	XP_016865456.1:p.Asp4771Ala
XM_017009968.2:c.14408A>C	XP_016865457.1:p.Asp4803Ala
XM_017009969.2:c.14408A>C	XP_016865458.1:p.Asp4803Ala
XM_017009970.2:c.14408A>C	XP_016865459.1:p.Asp4803Ala
XM_017009971.2:c.14408A>C	XP_016865460.1:p.Asp4803Ala
XM_017009972.1:c.7526A>C	XP_016865461.1:p.Asp2509Ala
XM_017009973.1:c.7505A>C	XP_016865462.1:p.Asp2502Ala
NR_003149.2:n.14403A>C