Canonical Allele Identifier: CA631723691

Gene: INSR

Linked Data

• dbSNP Id: rs1296356282
• gnomAD v2: 19-7132059-T-TCAAGGC
• gnomAD v3: 19-7132048-T-TCAAGGC
• gnomAD v4: 19-7132048-T-TCAAGGC
• MyVariant Identifiers: chr19:g.7132059_7132060insCAAGGC (hg19) ; chr19:g.7132048_7132049insCAAGGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132051_7132056dup , CM000681.2:g.7132051_7132056dup	GRCh38
NC_000019.9:g.7132062_7132067dup , CM000681.1:g.7132062_7132067dup	GRCh37
NC_000019.8:g.7083062_7083067dup	NCBI36
NG_008852.2:g.166947_166952dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2842+104_2842+109dup MANE Select	ENSP00000303830.4:n.2842+104_2842+109dup
ENST00000302850.9:c.2842+104_2842+109dup	ENSP00000303830.4:n.2842+104_2842+109dup
ENST00000341500.9:c.2806+104_2806+109dup	ENSP00000342838.4:n.2806+104_2806+109dup
NM_000208.2:c.2842+104_2842+109dup	NP_000199.2:n.2842+104_2842+109dup
NM_000208.3:c.2842+104_2842+109dup	NP_000199.2:n.2842+104_2842+109dup
NM_001079817.1:c.2806+104_2806+109dup	NP_001073285.1:n.2806+104_2806+109dup
NM_001079817.2:c.2806+104_2806+109dup	NP_001073285.1:n.2806+104_2806+109dup
XM_011527988.1:c.2920+104_2920+109dup	XP_011526290.1:n.2920+104_2920+109dup
XM_011527989.1:c.2884+104_2884+109dup	XP_011526291.1:n.2884+104_2884+109dup
XM_011527988.2:c.2842+104_2842+109dup	XP_011526290.2:n.2842+104_2842+109dup
XM_011527989.3:c.2806+104_2806+109dup	XP_011526291.2:n.2806+104_2806+109dup
NM_000208.4:c.2842+104_2842+109dup MANE Select	NP_000199.2:n.2842+104_2842+109dup
NM_001079817.3:c.2806+104_2806+109dup	NP_001073285.1:n.2806+104_2806+109dup