Canonical Allele Identifier: CA124244
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7131614_7132859del , CM000681.2:g.7131614_7132859del GRCh38
NC_000019.9:g.7131625_7132870del , CM000681.1:g.7131625_7132870del GRCh37
NC_000019.8:g.7082625_7083870del NCBI36
NG_008852.2:g.166142_167387del

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.2683-542_2842+544del
ENST00000302850.9:c.2683-542_2842+544del
ENST00000341500.9:c.2647-542_2806+544del
NM_000208.2:c.2683-542_2842+544del
NM_000208.3:c.2683-542_2842+544del
NM_001079817.1:c.2647-542_2806+544del
NM_001079817.2:c.2647-542_2806+544del
XM_011527988.1:c.2761-542_2920+544del
XM_011527989.1:c.2725-542_2884+544del
XM_011527988.2:c.2683-542_2842+544del
XM_011527989.3:c.2647-542_2806+544del
NM_000208.4:c.2683-542_2842+544del
NM_001079817.3:c.2647-542_2806+544del