Canonical Allele Identifier: CA993136114

Gene: INSR

Linked Data

• dbSNP Id: rs1973399991
• gnomAD v3: 19-7152575-T-TCTTAGATCTTGCC
• gnomAD v4: 19-7152575-T-TCTTAGATCTTGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7152578_7152579insAGATCTTGCCCTT , CM000681.2:g.7152578_7152579insAGATCTTGCCCTT	GRCh38
NC_000019.9:g.7152589_7152590insAGATCTTGCCCTT , CM000681.1:g.7152589_7152590insAGATCTTGCCCTT	GRCh37
NC_000019.8:g.7103589_7103590insAGATCTTGCCCTT	NCBI36
NG_008852.2:g.146425_146426insGGCAAGATCTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2231+150_2231+151insGGCAAGATCTAAG MANE Select	ENSP00000303830.4:n.2231+150_2231+151insGGCAAGATCTAAG
ENST00000302850.9:c.2231+150_2231+151insGGCAAGATCTAAG	ENSP00000303830.4:n.2231+150_2231+151insGGCAAGATCTAAG
ENST00000341500.9:c.2231+150_2231+151insGGCAAGATCTAAG	ENSP00000342838.4:n.2231+150_2231+151insGGCAAGATCTAAG
ENST00000598216.1:n.2356_2357insGGCAAGATCTAAG
NM_000208.2:c.2231+150_2231+151insGGCAAGATCTAAG	NP_000199.2:n.2231+150_2231+151insGGCAAGATCTAAG
NM_000208.3:c.2231+150_2231+151insGGCAAGATCTAAG	NP_000199.2:n.2231+150_2231+151insGGCAAGATCTAAG
NM_001079817.1:c.2231+150_2231+151insGGCAAGATCTAAG	NP_001073285.1:n.2231+150_2231+151insGGCAAGATCTAAG
NM_001079817.2:c.2231+150_2231+151insGGCAAGATCTAAG	NP_001073285.1:n.2231+150_2231+151insGGCAAGATCTAAG
XM_011527988.1:c.2309+150_2309+151insGGCAAGATCTAAG	XP_011526290.1:n.2309+150_2309+151insGGCAAGATCTAAG
XM_011527989.1:c.2309+150_2309+151insGGCAAGATCTAAG	XP_011526291.1:n.2309+150_2309+151insGGCAAGATCTAAG
XM_011527988.2:c.2231+150_2231+151insGGCAAGATCTAAG	XP_011526290.2:n.2231+150_2231+151insGGCAAGATCTAAG
XM_011527989.3:c.2231+150_2231+151insGGCAAGATCTAAG	XP_011526291.2:n.2231+150_2231+151insGGCAAGATCTAAG
NM_000208.4:c.2231+150_2231+151insGGCAAGATCTAAG MANE Select	NP_000199.2:n.2231+150_2231+151insGGCAAGATCTAAG
NM_001079817.3:c.2231+150_2231+151insGGCAAGATCTAAG	NP_001073285.1:n.2231+150_2231+151insGGCAAGATCTAAG