Canonical Allele Identifier: CA920049235

Gene: INSR

Linked Data

• dbSNP Id: rs35434645
• gnomAD v3: 19-7116767-TGG-T
• gnomAD v4: 19-7116767-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116772_7116773del , CM000681.2:g.7116772_7116773del	GRCh38
NC_000019.9:g.7116783_7116784del , CM000681.1:g.7116783_7116784del	GRCh37
NC_000019.8:g.7067783_7067784del	NCBI36
NG_008852.2:g.182232_182233del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.*287_*288del MANE Select	ENSP00000303830.4:n.*287_*288del
ENST00000302850.9:c.*287_*288del	ENSP00000303830.4:n.*287_*288del
ENST00000341500.9:c.*287_*288del	ENSP00000342838.4:n.*287_*288del
NM_000208.2:c.*287_*288del	NP_000199.2:n.*287_*288del
NM_000208.3:c.*287_*288del	NP_000199.2:n.*287_*288del
NM_001079817.1:c.*287_*288del	NP_001073285.1:n.*287_*288del
NM_001079817.2:c.*287_*288del	NP_001073285.1:n.*287_*288del
XM_011527988.1:c.*287_*288del	XP_011526290.1:n.*287_*288del
XM_011527989.1:c.*287_*288del	XP_011526291.1:n.*287_*288del
XM_011527988.2:c.*287_*288del	XP_011526290.2:n.*287_*288del
XM_011527989.3:c.*287_*288del	XP_011526291.2:n.*287_*288del
NM_000208.4:c.*287_*288del MANE Select	NP_000199.2:n.*287_*288del
NM_001079817.3:c.*287_*288del	NP_001073285.1:n.*287_*288del