Canonical Allele Identifier: CA2830538949

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823737_90823738insG , CM000667.2:g.90823737_90823738insG	GRCh38
NC_000005.9:g.90119554_90119555insG , CM000667.1:g.90119554_90119555insG	GRCh37
NC_000005.8:g.90155310_90155311insG	NCBI36
NG_007083.1:g.269938_269939insG
NG_007083.2:g.299394_299395insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16368+141_16368+142insG MANE Select	ENSP00000384582.2:n.16368+141_16368+142insG
ENST00000425867.3:c.5322+141_5322+142insG	ENSP00000392618.3:n.5322+141_5322+142insG
ENST00000638510.1:n.3635+141_3635+142insG
ENST00000639431.1:c.265+147528_265+147529insG	ENSP00000491057.1:n.265+147528_265+147529insG
ENST00000640061.1:n.128+1555_128+1556insG
ENST00000640407.1:c.2778+141_2778+142insG	ENSP00000491425.1:n.2778+141_2778+142insG
ENST00000405460.6:c.16368+141_16368+142insG	ENSP00000384582.2:n.16368+141_16368+142insG
ENST00000425867.2:c.3351+141_3351+142insG	ENSP00000392618.2:n.3351+141_3351+142insG
NM_032119.3:c.16368+141_16368+142insG	NP_115495.3:n.16368+141_16368+142insG
NR_003149.1:n.16381+141_16381+142insG
XM_011543675.1:c.16365+141_16365+142insG	XP_011541977.1:n.16365+141_16365+142insG
XM_011543676.1:c.16287+141_16287+142insG	XP_011541978.1:n.16287+141_16287+142insG
XM_011543677.1:c.13671+141_13671+142insG	XP_011541979.1:n.13671+141_13671+142insG
NM_032119.4:c.16368+141_16368+142insG MANE Select	NP_115495.3:n.16368+141_16368+142insG
XM_017009963.2:c.16389+141_16389+142insG	XP_016865452.1:n.16389+141_16389+142insG
XM_017009964.2:c.16386+141_16386+142insG	XP_016865453.1:n.16386+141_16386+142insG
XM_017009965.1:c.16386+141_16386+142insG	XP_016865454.1:n.16386+141_16386+142insG
XM_017009966.2:c.16308+141_16308+142insG	XP_016865455.1:n.16308+141_16308+142insG
XM_017009967.1:c.16293+141_16293+142insG	XP_016865456.1:n.16293+141_16293+142insG
XM_017009968.2:c.16209+141_16209+142insG	XP_016865457.1:n.16209+141_16209+142insG
XM_017009969.2:c.16389+141_16389+142insG	XP_016865458.1:n.16389+141_16389+142insG
XM_017009972.1:c.9507+141_9507+142insG	XP_016865461.1:n.9507+141_9507+142insG
XM_017009973.1:c.9486+141_9486+142insG	XP_016865462.1:n.9486+141_9486+142insG
NR_003149.2:n.16384+141_16384+142insG