Canonical Allele Identifier: CA9136044

Gene: INSR

Linked Data

• ClinVar Variation Id: 783815
• ClinVar RCV Id: RCV000965418 ; RCV001819062 ; RCV002503031
• dbSNP Id: rs766817873
• ExAC: 19:7184654 GA / G
• gnomAD v2: 19-7184654-GA-G
• gnomAD v3: 19-7184643-GA-G
• gnomAD v4: 19-7184643-GA-G
• MyVariant Identifiers: chr19:g.7184655del (hg19) ; chr19:g.7184644del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184644del , CM000681.2:g.7184644del	GRCh38
NC_000019.9:g.7184655del , CM000681.1:g.7184655del	GRCh37
NC_000019.8:g.7135655del	NCBI36
NG_008852.2:g.114357del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.653-7del MANE Select	ENSP00000303830.4:n.653-7del
ENST00000302850.9:c.653-7del	ENSP00000303830.4:n.653-7del
ENST00000341500.9:c.653-7del	ENSP00000342838.4:n.653-7del
ENST00000598216.1:n.628-7del
NM_000208.2:c.653-7del	NP_000199.2:n.653-7del
NM_000208.3:c.653-7del	NP_000199.2:n.653-7del
NM_001079817.1:c.653-7del	NP_001073285.1:n.653-7del
NM_001079817.2:c.653-7del	NP_001073285.1:n.653-7del
XM_011527988.1:c.731-7del	XP_011526290.1:n.731-7del
XM_011527989.1:c.731-7del	XP_011526291.1:n.731-7del
XM_011527988.2:c.653-7del	XP_011526290.2:n.653-7del
XM_011527989.3:c.653-7del	XP_011526291.2:n.653-7del
NM_000208.4:c.653-7del MANE Select	NP_000199.2:n.653-7del
NM_001079817.3:c.653-7del	NP_001073285.1:n.653-7del