Canonical Allele Identifier: CA360425689

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119368G>C (hg19) ; chr5:g.90823551G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823551G>C , CM000667.2:g.90823551G>C	GRCh38
NC_000005.9:g.90119368G>C , CM000667.1:g.90119368G>C	GRCh37
NC_000005.8:g.90155124G>C	NCBI36
NG_007083.1:g.269752G>C
NG_007083.2:g.299208G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16323G>C MANE Select	ENSP00000384582.2:p.Met5441Ile
ENST00000425867.3:c.5277G>C	ENSP00000392618.3:p.Met1759Ile
ENST00000638510.1:n.3590G>C
ENST00000639431.1:c.265+147342G>C	ENSP00000491057.1:n.265+147342G>C
ENST00000640061.1:n.128+1369G>C
ENST00000640407.1:c.2733G>C	ENSP00000491425.1:p.Met911Ile
ENST00000405460.6:c.16323G>C	ENSP00000384582.2:p.Met5441Ile
ENST00000425867.2:c.3306G>C	ENSP00000392618.2:p.Met1102Ile
NM_032119.3:c.16323G>C	NP_115495.3:p.Met5441Ile
NR_003149.1:n.16336G>C
XM_011543675.1:c.16320G>C	XP_011541977.1:p.Met5440Ile
XM_011543676.1:c.16242G>C	XP_011541978.1:p.Met5414Ile
XM_011543677.1:c.13626G>C	XP_011541979.1:p.Met4542Ile
NM_032119.4:c.16323G>C MANE Select	NP_115495.3:p.Met5441Ile
XM_017009963.2:c.16344G>C	XP_016865452.1:p.Met5448Ile
XM_017009964.2:c.16341G>C	XP_016865453.1:p.Met5447Ile
XM_017009965.1:c.16341G>C	XP_016865454.1:p.Met5447Ile
XM_017009966.2:c.16263G>C	XP_016865455.1:p.Met5421Ile
XM_017009967.1:c.16248G>C	XP_016865456.1:p.Met5416Ile
XM_017009968.2:c.16164G>C	XP_016865457.1:p.Met5388Ile
XM_017009969.2:c.16344G>C	XP_016865458.1:p.Met5448Ile
XM_017009972.1:c.9462G>C	XP_016865461.1:p.Met3154Ile
XM_017009973.1:c.9441G>C	XP_016865462.1:p.Met3147Ile
NR_003149.2:n.16339G>C