Canonical Allele Identifier: CA2320780891

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7152512_7152514delinsCTT , CM000681.2:g.7152512_7152514delinsCTT	GRCh38
NC_000019.9:g.7152523_7152525delinsCTT , CM000681.1:g.7152523_7152525delinsCTT	GRCh37
NC_000019.8:g.7103523_7103525delinsCTT	NCBI36
NG_008852.2:g.146487_146489delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2231+212_2231+214delinsAAG MANE Select	ENSP00000303830.4:n.2231+212_2231+214delinsAAG
ENST00000302850.9:c.2231+212_2231+214delinsAAG	ENSP00000303830.4:n.2231+212_2231+214delinsAAG
ENST00000341500.9:c.2231+212_2231+214delinsAAG	ENSP00000342838.4:n.2231+212_2231+214delinsAAG
ENST00000598216.1:n.2418_2420delinsAAG
NM_000208.2:c.2231+212_2231+214delinsAAG	NP_000199.2:n.2231+212_2231+214delinsAAG
NM_000208.3:c.2231+212_2231+214delinsAAG	NP_000199.2:n.2231+212_2231+214delinsAAG
NM_001079817.1:c.2231+212_2231+214delinsAAG	NP_001073285.1:n.2231+212_2231+214delinsAAG
NM_001079817.2:c.2231+212_2231+214delinsAAG	NP_001073285.1:n.2231+212_2231+214delinsAAG
XM_011527988.1:c.2309+212_2309+214delinsAAG	XP_011526290.1:n.2309+212_2309+214delinsAAG
XM_011527989.1:c.2309+212_2309+214delinsAAG	XP_011526291.1:n.2309+212_2309+214delinsAAG
XM_011527988.2:c.2231+212_2231+214delinsAAG	XP_011526290.2:n.2231+212_2231+214delinsAAG
XM_011527989.3:c.2231+212_2231+214delinsAAG	XP_011526291.2:n.2231+212_2231+214delinsAAG
NM_000208.4:c.2231+212_2231+214delinsAAG MANE Select	NP_000199.2:n.2231+212_2231+214delinsAAG
NM_001079817.3:c.2231+212_2231+214delinsAAG	NP_001073285.1:n.2231+212_2231+214delinsAAG