Canonical Allele Identifier: CA2517925431

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7211815_7211816insTGC , CM000681.2:g.7211815_7211816insTGC	GRCh38
NC_000019.9:g.7211826_7211827insTGC , CM000681.1:g.7211826_7211827insTGC	GRCh37
NC_000019.8:g.7162826_7162827insTGC	NCBI36
NG_008852.2:g.87185_87186insGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27179_653-27178insGCA MANE Select	ENSP00000303830.4:n.653-27179_653-27178insGCA
ENST00000302850.9:c.653-27179_653-27178insGCA	ENSP00000303830.4:n.653-27179_653-27178insGCA
ENST00000341500.9:c.653-27179_653-27178insGCA	ENSP00000342838.4:n.653-27179_653-27178insGCA
ENST00000598216.1:n.628-27179_628-27178insGCA
NM_000208.2:c.653-27179_653-27178insGCA	NP_000199.2:n.653-27179_653-27178insGCA
NM_000208.3:c.653-27179_653-27178insGCA	NP_000199.2:n.653-27179_653-27178insGCA
NM_001079817.1:c.653-27179_653-27178insGCA	NP_001073285.1:n.653-27179_653-27178insGCA
NM_001079817.2:c.653-27179_653-27178insGCA	NP_001073285.1:n.653-27179_653-27178insGCA
XM_011527988.1:c.731-27179_731-27178insGCA	XP_011526290.1:n.731-27179_731-27178insGCA
XM_011527989.1:c.731-27179_731-27178insGCA	XP_011526291.1:n.731-27179_731-27178insGCA
XM_011527988.2:c.653-27179_653-27178insGCA	XP_011526290.2:n.653-27179_653-27178insGCA
XM_011527989.3:c.653-27179_653-27178insGCA	XP_011526291.2:n.653-27179_653-27178insGCA
NM_000208.4:c.653-27179_653-27178insGCA MANE Select	NP_000199.2:n.653-27179_653-27178insGCA
NM_001079817.3:c.653-27179_653-27178insGCA	NP_001073285.1:n.653-27179_653-27178insGCA