Canonical Allele Identifier: CA445436515

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119290A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823473A>C , CM000667.2:g.90823473A>C	GRCh38
NC_000005.9:g.90119290A>C , CM000667.1:g.90119290A>C	GRCh37
NC_000005.8:g.90155046A>C	NCBI36
NG_007083.1:g.269674A>C
NG_007083.2:g.299130A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16245A>C MANE Select	ENSP00000384582.2:p.Thr5415=
ENST00000425867.3:c.5199A>C	ENSP00000392618.3:p.Thr1733=
ENST00000638510.1:n.3512A>C
ENST00000639431.1:c.265+147264A>C	ENSP00000491057.1:n.265+147264A>C
ENST00000640061.1:n.128+1291A>C
ENST00000640407.1:c.2655A>C	ENSP00000491425.1:p.Thr885=
ENST00000405460.6:c.16245A>C	ENSP00000384582.2:p.Thr5415=
ENST00000425867.2:c.3228A>C	ENSP00000392618.2:p.Thr1076=
NM_032119.3:c.16245A>C	NP_115495.3:p.Thr5415=
NR_003149.1:n.16258A>C
XM_011543675.1:c.16242A>C	XP_011541977.1:p.Thr5414=
XM_011543676.1:c.16164A>C	XP_011541978.1:p.Thr5388=
XM_011543677.1:c.13548A>C	XP_011541979.1:p.Thr4516=
NM_032119.4:c.16245A>C MANE Select	NP_115495.3:p.Thr5415=
XM_017009963.2:c.16266A>C	XP_016865452.1:p.Thr5422=
XM_017009964.2:c.16263A>C	XP_016865453.1:p.Thr5421=
XM_017009965.1:c.16263A>C	XP_016865454.1:p.Thr5421=
XM_017009966.2:c.16185A>C	XP_016865455.1:p.Thr5395=
XM_017009967.1:c.16170A>C	XP_016865456.1:p.Thr5390=
XM_017009968.2:c.16086A>C	XP_016865457.1:p.Thr5362=
XM_017009969.2:c.16266A>C	XP_016865458.1:p.Thr5422=
XM_017009972.1:c.9384A>C	XP_016865461.1:p.Thr3128=
XM_017009973.1:c.9363A>C	XP_016865462.1:p.Thr3121=
NR_003149.2:n.16261A>C