Canonical Allele Identifier: CA2587920961

Gene: INSR

Linked Data

• gnomAD v4: 19-7116981-A-ACCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116981_7116982insCCAT , CM000681.2:g.7116981_7116982insCCAT	GRCh38
NC_000019.9:g.7116992_7116993insCCAT , CM000681.1:g.7116992_7116993insCCAT	GRCh37
NC_000019.8:g.7067992_7067993insCCAT	NCBI36
NG_008852.2:g.182019_182020insATGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.*74_*75insATGG MANE Select	ENSP00000303830.4:n.*74_*75insATGG
ENST00000302850.9:c.*74_*75insATGG	ENSP00000303830.4:n.*74_*75insATGG
ENST00000341500.9:c.*74_*75insATGG	ENSP00000342838.4:n.*74_*75insATGG
NM_000208.2:c.*74_*75insATGG	NP_000199.2:n.*74_*75insATGG
NM_000208.3:c.*74_*75insATGG	NP_000199.2:n.*74_*75insATGG
NM_001079817.1:c.*74_*75insATGG	NP_001073285.1:n.*74_*75insATGG
NM_001079817.2:c.*74_*75insATGG	NP_001073285.1:n.*74_*75insATGG
XM_011527988.1:c.*74_*75insATGG	XP_011526290.1:n.*74_*75insATGG
XM_011527989.1:c.*74_*75insATGG	XP_011526291.1:n.*74_*75insATGG
XM_011527988.2:c.*74_*75insATGG	XP_011526290.2:n.*74_*75insATGG
XM_011527989.3:c.*74_*75insATGG	XP_011526291.2:n.*74_*75insATGG
NM_000208.4:c.*74_*75insATGG MANE Select	NP_000199.2:n.*74_*75insATGG
NM_001079817.3:c.*74_*75insATGG	NP_001073285.1:n.*74_*75insATGG