Canonical Allele Identifier: CA993113729

Gene: INSR

Linked Data

• gnomAD v3: 19-7116952-TTG-T
• gnomAD v4: 19-7116952-TTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116953_7116954del , CM000681.2:g.7116953_7116954del	GRCh38
NC_000019.9:g.7116964_7116965del , CM000681.1:g.7116964_7116965del	GRCh37
NC_000019.8:g.7067964_7067965del	NCBI36
NG_008852.2:g.182047_182048del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.*102_*103del MANE Select	ENSP00000303830.4:n.*102_*103del
ENST00000302850.9:c.*102_*103del	ENSP00000303830.4:n.*102_*103del
ENST00000341500.9:c.*102_*103del	ENSP00000342838.4:n.*102_*103del
NM_000208.2:c.*102_*103del	NP_000199.2:n.*102_*103del
NM_000208.3:c.*102_*103del	NP_000199.2:n.*102_*103del
NM_001079817.1:c.*102_*103del	NP_001073285.1:n.*102_*103del
NM_001079817.2:c.*102_*103del	NP_001073285.1:n.*102_*103del
XM_011527988.1:c.*102_*103del	XP_011526290.1:n.*102_*103del
XM_011527989.1:c.*102_*103del	XP_011526291.1:n.*102_*103del
XM_011527988.2:c.*102_*103del	XP_011526290.2:n.*102_*103del
XM_011527989.3:c.*102_*103del	XP_011526291.2:n.*102_*103del
NM_000208.4:c.*102_*103del MANE Select	NP_000199.2:n.*102_*103del
NM_001079817.3:c.*102_*103del	NP_001073285.1:n.*102_*103del