Canonical Allele Identifier: CA2576594894

Gene: INSR

Linked Data

• gnomAD v4: 19-7116959-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116961del , CM000681.2:g.7116961del	GRCh38
NC_000019.9:g.7116972del , CM000681.1:g.7116972del	GRCh37
NC_000019.8:g.7067972del	NCBI36
NG_008852.2:g.182041del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.*96del MANE Select	ENSP00000303830.4:n.*96del
ENST00000302850.9:c.*96del	ENSP00000303830.4:n.*96del
ENST00000341500.9:c.*96del	ENSP00000342838.4:n.*96del
NM_000208.2:c.*96del	NP_000199.2:n.*96del
NM_000208.3:c.*96del	NP_000199.2:n.*96del
NM_001079817.1:c.*96del	NP_001073285.1:n.*96del
NM_001079817.2:c.*96del	NP_001073285.1:n.*96del
XM_011527988.1:c.*96del	XP_011526290.1:n.*96del
XM_011527989.1:c.*96del	XP_011526291.1:n.*96del
XM_011527988.2:c.*96del	XP_011526290.2:n.*96del
XM_011527989.3:c.*96del	XP_011526291.2:n.*96del
NM_000208.4:c.*96del MANE Select	NP_000199.2:n.*96del
NM_001079817.3:c.*96del	NP_001073285.1:n.*96del