Canonical Allele Identifier: CA2813464198

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184661_7184662insAGAA , CM000681.2:g.7184661_7184662insAGAA	GRCh38
NC_000019.9:g.7184672_7184673insAGAA , CM000681.1:g.7184672_7184673insAGAA	GRCh37
NC_000019.8:g.7135672_7135673insAGAA	NCBI36
NG_008852.2:g.114339_114340insTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-25_653-24insTTCT MANE Select	ENSP00000303830.4:n.653-25_653-24insTTCT
ENST00000302850.9:c.653-25_653-24insTTCT	ENSP00000303830.4:n.653-25_653-24insTTCT
ENST00000341500.9:c.653-25_653-24insTTCT	ENSP00000342838.4:n.653-25_653-24insTTCT
ENST00000598216.1:n.628-25_628-24insTTCT
NM_000208.2:c.653-25_653-24insTTCT	NP_000199.2:n.653-25_653-24insTTCT
NM_000208.3:c.653-25_653-24insTTCT	NP_000199.2:n.653-25_653-24insTTCT
NM_001079817.1:c.653-25_653-24insTTCT	NP_001073285.1:n.653-25_653-24insTTCT
NM_001079817.2:c.653-25_653-24insTTCT	NP_001073285.1:n.653-25_653-24insTTCT
XM_011527988.1:c.731-25_731-24insTTCT	XP_011526290.1:n.731-25_731-24insTTCT
XM_011527989.1:c.731-25_731-24insTTCT	XP_011526291.1:n.731-25_731-24insTTCT
XM_011527988.2:c.653-25_653-24insTTCT	XP_011526290.2:n.653-25_653-24insTTCT
XM_011527989.3:c.653-25_653-24insTTCT	XP_011526291.2:n.653-25_653-24insTTCT
NM_000208.4:c.653-25_653-24insTTCT MANE Select	NP_000199.2:n.653-25_653-24insTTCT
NM_001079817.3:c.653-25_653-24insTTCT	NP_001073285.1:n.653-25_653-24insTTCT