Canonical Allele Identifier: CA137993

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745073T>C , CM000667.2:g.90745073T>C	GRCh38
NC_000005.9:g.90040890T>C , CM000667.1:g.90040890T>C	GRCh37
NC_000005.8:g.90076646T>C	NCBI36
NG_007083.1:g.191274T>C
NG_007083.2:g.220730T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10577T>C MANE Select	ENSP00000384582.2:p.Met3526Thr
ENST00000639431.1:c.265+68864T>C	ENSP00000491057.1:n.265+68864T>C
ENST00000640374.1:n.3721T>C
ENST00000640464.1:n.996T>C
ENST00000405460.6:c.10577T>C	ENSP00000384582.2:p.Met3526Thr
ENST00000509621.1:c.3274T>C
NM_032119.3:c.10577T>C	NP_115495.3:p.Met3526Thr
NR_003149.1:n.10590T>C
XM_011543675.1:c.10574T>C	XP_011541977.1:p.Met3525Thr
XM_011543676.1:c.10496T>C	XP_011541978.1:p.Met3499Thr
XM_011543677.1:c.7880T>C	XP_011541979.1:p.Met2627Thr
XM_011543678.1:c.10577T>C	XP_011541980.1:p.Met3526Thr
XM_011543679.1:c.10577T>C	XP_011541981.1:p.Met3526Thr
NM_032119.4:c.10577T>C MANE Select	NP_115495.3:p.Met3526Thr
XM_017009963.2:c.10598T>C	XP_016865452.1:p.Met3533Thr
XM_017009964.2:c.10595T>C	XP_016865453.1:p.Met3532Thr
XM_017009965.1:c.10595T>C	XP_016865454.1:p.Met3532Thr
XM_017009966.2:c.10517T>C	XP_016865455.1:p.Met3506Thr
XM_017009967.1:c.10502T>C	XP_016865456.1:p.Met3501Thr
XM_017009968.2:c.10598T>C	XP_016865457.1:p.Met3533Thr
XM_017009969.2:c.10598T>C	XP_016865458.1:p.Met3533Thr
XM_017009970.2:c.10598T>C	XP_016865459.1:p.Met3533Thr
XM_017009971.2:c.10598T>C	XP_016865460.1:p.Met3533Thr
XM_017009972.1:c.3716T>C	XP_016865461.1:p.Met1239Thr
XM_017009973.1:c.3695T>C	XP_016865462.1:p.Met1232Thr
XM_017009974.2:c.10598T>C	XP_016865463.1:p.Met3533Thr
NR_003149.2:n.10593T>C