Canonical Allele Identifier: CA2587925331

Gene: INSR

Linked Data

• gnomAD v4: 19-7166548-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166548_7166549insC , CM000681.2:g.7166548_7166549insC	GRCh38
NC_000019.9:g.7166559_7166560insC , CM000681.1:g.7166559_7166560insC	GRCh37
NC_000019.8:g.7117559_7117560insC	NCBI36
NG_008852.2:g.132452_132453insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1611-145_1611-144insG MANE Select	ENSP00000303830.4:n.1611-145_1611-144insG
ENST00000302850.9:c.1611-145_1611-144insG	ENSP00000303830.4:n.1611-145_1611-144insG
ENST00000341500.9:c.1611-145_1611-144insG	ENSP00000342838.4:n.1611-145_1611-144insG
ENST00000598216.1:n.1586-145_1586-144insG
ENST00000600492.1:c.12-145_12-144insG	ENSP00000473170.1:n.12-145_12-144insG
NM_000208.2:c.1611-145_1611-144insG	NP_000199.2:n.1611-145_1611-144insG
NM_000208.3:c.1611-145_1611-144insG	NP_000199.2:n.1611-145_1611-144insG
NM_001079817.1:c.1611-145_1611-144insG	NP_001073285.1:n.1611-145_1611-144insG
NM_001079817.2:c.1611-145_1611-144insG	NP_001073285.1:n.1611-145_1611-144insG
XM_011527988.1:c.1689-145_1689-144insG	XP_011526290.1:n.1689-145_1689-144insG
XM_011527989.1:c.1689-145_1689-144insG	XP_011526291.1:n.1689-145_1689-144insG
XM_011527988.2:c.1611-145_1611-144insG	XP_011526290.2:n.1611-145_1611-144insG
XM_011527989.3:c.1611-145_1611-144insG	XP_011526291.2:n.1611-145_1611-144insG
NM_000208.4:c.1611-145_1611-144insG MANE Select	NP_000199.2:n.1611-145_1611-144insG
NM_001079817.3:c.1611-145_1611-144insG	NP_001073285.1:n.1611-145_1611-144insG