Canonical Allele Identifier: CA3341454

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90781519T>C , CM000667.2:g.90781519T>C	GRCh38
NC_000005.9:g.90077336T>C , CM000667.1:g.90077336T>C	GRCh37
NC_000005.8:g.90113092T>C	NCBI36
NG_007083.1:g.227720T>C
NG_007083.2:g.257176T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13172T>C MANE Select	NP_115495.3:p.Met4391Thr
ENST00000405460.9:c.13172T>C MANE Select	ENSP00000384582.2:p.Met4391Thr
NM_032119.3:c.13172T>C	NP_115495.3:p.Met4391Thr
NR_003149.1:n.13185T>C
NR_003149.2:n.13188T>C
ENST00000405460.6:c.13172T>C	ENSP00000384582.2:p.Met4391Thr
ENST00000425867.2:c.155T>C	ENSP00000392618.2:p.Met52Thr
ENST00000425867.3:c.2126T>C	ENSP00000392618.3:p.Met709Thr
ENST00000638510.1:n.439T>C
ENST00000639431.1:c.265+105310T>C	ENSP00000491057.1:n.265+105310T>C
XM_011543675.1:c.13169T>C	XP_011541977.1:p.Met4390Thr
XM_011543676.1:c.13091T>C	XP_011541978.1:p.Met4364Thr
XM_011543677.1:c.10475T>C	XP_011541979.1:p.Met3492Thr
XM_011543678.1:c.13172T>C	XP_011541980.1:p.Met4391Thr
XM_017009963.2:c.13193T>C	XP_016865452.1:p.Met4398Thr
XM_017009964.2:c.13190T>C	XP_016865453.1:p.Met4397Thr
XM_017009965.1:c.13190T>C	XP_016865454.1:p.Met4397Thr
XM_017009966.2:c.13112T>C	XP_016865455.1:p.Met4371Thr
XM_017009967.1:c.13097T>C	XP_016865456.1:p.Met4366Thr
XM_017009968.2:c.13193T>C	XP_016865457.1:p.Met4398Thr
XM_017009969.2:c.13193T>C	XP_016865458.1:p.Met4398Thr
XM_017009970.2:c.13193T>C	XP_016865459.1:p.Met4398Thr
XM_017009971.2:c.13193T>C	XP_016865460.1:p.Met4398Thr
XM_017009972.1:c.6311T>C	XP_016865461.1:p.Met2104Thr
XM_017009973.1:c.6290T>C	XP_016865462.1:p.Met2097Thr