Canonical Allele Identifier: CA360425789

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119412A>C (hg19) ; chr5:g.90823595A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823595A>C , CM000667.2:g.90823595A>C	GRCh38
NC_000005.9:g.90119412A>C , CM000667.1:g.90119412A>C	GRCh37
NC_000005.8:g.90155168A>C	NCBI36
NG_007083.1:g.269796A>C
NG_007083.2:g.299252A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16367A>C MANE Select	ENSP00000384582.2:p.Lys5456Thr
ENST00000425867.3:c.5321A>C	ENSP00000392618.3:p.Lys1774Thr
ENST00000638510.1:n.3634A>C
ENST00000639431.1:c.265+147386A>C	ENSP00000491057.1:n.265+147386A>C
ENST00000640061.1:n.128+1413A>C
ENST00000640407.1:c.2777A>C	ENSP00000491425.1:p.Lys926Thr
ENST00000405460.6:c.16367A>C	ENSP00000384582.2:p.Lys5456Thr
ENST00000425867.2:c.3350A>C	ENSP00000392618.2:p.Lys1117Thr
NM_032119.3:c.16367A>C	NP_115495.3:p.Lys5456Thr
NR_003149.1:n.16380A>C
XM_011543675.1:c.16364A>C	XP_011541977.1:p.Lys5455Thr
XM_011543676.1:c.16286A>C	XP_011541978.1:p.Lys5429Thr
XM_011543677.1:c.13670A>C	XP_011541979.1:p.Lys4557Thr
NM_032119.4:c.16367A>C MANE Select	NP_115495.3:p.Lys5456Thr
XM_017009963.2:c.16388A>C	XP_016865452.1:p.Lys5463Thr
XM_017009964.2:c.16385A>C	XP_016865453.1:p.Lys5462Thr
XM_017009965.1:c.16385A>C	XP_016865454.1:p.Lys5462Thr
XM_017009966.2:c.16307A>C	XP_016865455.1:p.Lys5436Thr
XM_017009967.1:c.16292A>C	XP_016865456.1:p.Lys5431Thr
XM_017009968.2:c.16208A>C	XP_016865457.1:p.Lys5403Thr
XM_017009969.2:c.16388A>C	XP_016865458.1:p.Lys5463Thr
XM_017009972.1:c.9506A>C	XP_016865461.1:p.Lys3169Thr
XM_017009973.1:c.9485A>C	XP_016865462.1:p.Lys3162Thr
NR_003149.2:n.16383A>C