Canonical Allele Identifier: CA2587926355

Gene: INSR

Linked Data

• gnomAD v4: 19-7184662-GGAAATAAATAAATAAATAAATAAAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184663_7184687del , CM000681.2:g.7184663_7184687del	GRCh38
NC_000019.9:g.7184674_7184698del , CM000681.1:g.7184674_7184698del	GRCh37
NC_000019.8:g.7135674_7135698del	NCBI36
NG_008852.2:g.114314_114338del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-50_653-26del MANE Select	ENSP00000303830.4:n.653-50_653-26del
ENST00000302850.9:c.653-50_653-26del	ENSP00000303830.4:n.653-50_653-26del
ENST00000341500.9:c.653-50_653-26del	ENSP00000342838.4:n.653-50_653-26del
ENST00000598216.1:n.628-50_628-26del
NM_000208.2:c.653-50_653-26del	NP_000199.2:n.653-50_653-26del
NM_000208.3:c.653-50_653-26del	NP_000199.2:n.653-50_653-26del
NM_001079817.1:c.653-50_653-26del	NP_001073285.1:n.653-50_653-26del
NM_001079817.2:c.653-50_653-26del	NP_001073285.1:n.653-50_653-26del
XM_011527988.1:c.731-50_731-26del	XP_011526290.1:n.731-50_731-26del
XM_011527989.1:c.731-50_731-26del	XP_011526291.1:n.731-50_731-26del
XM_011527988.2:c.653-50_653-26del	XP_011526290.2:n.653-50_653-26del
XM_011527989.3:c.653-50_653-26del	XP_011526291.2:n.653-50_653-26del
NM_000208.4:c.653-50_653-26del MANE Select	NP_000199.2:n.653-50_653-26del
NM_001079817.3:c.653-50_653-26del	NP_001073285.1:n.653-50_653-26del