Canonical Allele Identifier: CA884177925

Gene: INSR

Linked Data

• dbSNP Id: rs1417256070
• gnomAD v3: 19-7167872-C-CA
• gnomAD v4: 19-7167872-C-CA
• MyVariant Identifiers: chr19:g.7167883_7167884insA (hg19) ; chr19:g.7167872_7167873insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7167873dup , CM000681.2:g.7167873dup	GRCh38
NC_000019.9:g.7167884dup , CM000681.1:g.7167884dup	GRCh37
NC_000019.8:g.7118884dup	NCBI36
NG_008852.2:g.131128dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.1610+95dup MANE Select	ENSP00000303830.4:n.1610+95dup
ENST00000302850.9:c.1610+95dup	ENSP00000303830.4:n.1610+95dup
ENST00000341500.9:c.1610+95dup	ENSP00000342838.4:n.1610+95dup
ENST00000598216.1:n.1585+95dup
ENST00000600492.1:c.11+95dup	ENSP00000473170.1:n.11+95dup
NM_000208.2:c.1610+95dup	NP_000199.2:n.1610+95dup
NM_000208.3:c.1610+95dup	NP_000199.2:n.1610+95dup
NM_001079817.1:c.1610+95dup	NP_001073285.1:n.1610+95dup
NM_001079817.2:c.1610+95dup	NP_001073285.1:n.1610+95dup
XM_011527988.1:c.1688+95dup	XP_011526290.1:n.1688+95dup
XM_011527989.1:c.1688+95dup	XP_011526291.1:n.1688+95dup
XM_011527988.2:c.1610+95dup	XP_011526290.2:n.1610+95dup
XM_011527989.3:c.1610+95dup	XP_011526291.2:n.1610+95dup
NM_000208.4:c.1610+95dup MANE Select	NP_000199.2:n.1610+95dup
NM_001079817.3:c.1610+95dup	NP_001073285.1:n.1610+95dup