Canonical Allele Identifier: CA3341964

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810958T>C , CM000667.2:g.90810958T>C	GRCh38
NC_000005.9:g.90106775T>C , CM000667.1:g.90106775T>C	GRCh37
NC_000005.8:g.90142531T>C	NCBI36
NG_007083.1:g.257159T>C
NG_007083.2:g.286615T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15698T>C MANE Select	NP_115495.3:p.Met5233Thr
ENST00000405460.9:c.15698T>C MANE Select	ENSP00000384582.2:p.Met5233Thr
NM_032119.3:c.15698T>C	NP_115495.3:p.Met5233Thr
NR_003149.1:n.15711T>C
NR_003149.2:n.15714T>C
ENST00000405460.6:c.15698T>C	ENSP00000384582.2:p.Met5233Thr
ENST00000425867.2:c.2681T>C	ENSP00000392618.2:p.Met894Thr
ENST00000425867.3:c.4652T>C	ENSP00000392618.3:p.Met1551Thr
ENST00000638510.1:n.2965T>C
ENST00000639431.1:c.265+134749T>C	ENSP00000491057.1:n.265+134749T>C
ENST00000640407.1:c.2108T>C	ENSP00000491425.1:p.Met703Thr
XM_011543675.1:c.15695T>C	XP_011541977.1:p.Met5232Thr
XM_011543676.1:c.15617T>C	XP_011541978.1:p.Met5206Thr
XM_011543677.1:c.13001T>C	XP_011541979.1:p.Met4334Thr
XM_017009963.2:c.15719T>C	XP_016865452.1:p.Met5240Thr
XM_017009964.2:c.15716T>C	XP_016865453.1:p.Met5239Thr
XM_017009965.1:c.15716T>C	XP_016865454.1:p.Met5239Thr
XM_017009966.2:c.15638T>C	XP_016865455.1:p.Met5213Thr
XM_017009967.1:c.15623T>C	XP_016865456.1:p.Met5208Thr
XM_017009968.2:c.15539T>C	XP_016865457.1:p.Met5180Thr
XM_017009969.2:c.15719T>C	XP_016865458.1:p.Met5240Thr
XM_017009972.1:c.8837T>C	XP_016865461.1:p.Met2946Thr
XM_017009973.1:c.8816T>C	XP_016865462.1:p.Met2939Thr