Canonical Allele Identifier: CA2587920881

Gene: INSR

Linked Data

• gnomAD v4: 19-7116922-GAAATGTAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116924_7116931del , CM000681.2:g.7116924_7116931del	GRCh38
NC_000019.9:g.7116935_7116942del , CM000681.1:g.7116935_7116942del	GRCh37
NC_000019.8:g.7067935_7067942del	NCBI36
NG_008852.2:g.182071_182078del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.*126_*133del MANE Select	ENSP00000303830.4:n.*126_*133del
ENST00000302850.9:c.*126_*133del	ENSP00000303830.4:n.*126_*133del
ENST00000341500.9:c.*126_*133del	ENSP00000342838.4:n.*126_*133del
NM_000208.2:c.*126_*133del	NP_000199.2:n.*126_*133del
NM_000208.3:c.*126_*133del	NP_000199.2:n.*126_*133del
NM_001079817.1:c.*126_*133del	NP_001073285.1:n.*126_*133del
NM_001079817.2:c.*126_*133del	NP_001073285.1:n.*126_*133del
XM_011527988.1:c.*126_*133del	XP_011526290.1:n.*126_*133del
XM_011527989.1:c.*126_*133del	XP_011526291.1:n.*126_*133del
XM_011527988.2:c.*126_*133del	XP_011526290.2:n.*126_*133del
XM_011527989.3:c.*126_*133del	XP_011526291.2:n.*126_*133del
NM_000208.4:c.*126_*133del MANE Select	NP_000199.2:n.*126_*133del
NM_001079817.3:c.*126_*133del	NP_001073285.1:n.*126_*133del