Canonical Allele Identifier: CA993107651

Gene: INSR

Linked Data

• dbSNP Id: rs1972705998
• gnomAD v3: 19-7128767-TA-T
• gnomAD v4: 19-7128767-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128770del , CM000681.2:g.7128770del	GRCh38
NC_000019.9:g.7128781del , CM000681.1:g.7128781del	GRCh37
NC_000019.8:g.7079781del	NCBI36
NG_008852.2:g.170233del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2945+84del MANE Select	ENSP00000303830.4:n.2945+84del
ENST00000302850.9:c.2945+84del	ENSP00000303830.4:n.2945+84del
ENST00000341500.9:c.2909+84del	ENSP00000342838.4:n.2909+84del
NM_000208.2:c.2945+84del	NP_000199.2:n.2945+84del
NM_000208.3:c.2945+84del	NP_000199.2:n.2945+84del
NM_001079817.1:c.2909+84del	NP_001073285.1:n.2909+84del
NM_001079817.2:c.2909+84del	NP_001073285.1:n.2909+84del
XM_011527988.1:c.3020+84del	XP_011526290.1:n.3020+84del
XM_011527989.1:c.2984+84del	XP_011526291.1:n.2984+84del
XM_011527988.2:c.2942+84del	XP_011526290.2:n.2942+84del
XM_011527989.3:c.2906+84del	XP_011526291.2:n.2906+84del
NM_000208.4:c.2945+84del MANE Select	NP_000199.2:n.2945+84del
NM_001079817.3:c.2909+84del	NP_001073285.1:n.2909+84del