Canonical Allele Identifier: CA631723711

Gene: INSR

Linked Data

• dbSNP Id: rs780601620
• gnomAD v2: 19-7184653-A-AGG
• gnomAD v3: 19-7184642-A-AGG
• gnomAD v4: 19-7184642-A-AGG
• MyVariant Identifiers: chr19:g.7184653_7184654insGG (hg19) ; chr19:g.7184642_7184643insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184643_7184644insGG , CM000681.2:g.7184643_7184644insGG	GRCh38
NC_000019.9:g.7184654_7184655insGG , CM000681.1:g.7184654_7184655insGG	GRCh37
NC_000019.8:g.7135654_7135655insGG	NCBI36
NG_008852.2:g.114358_114359insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-6_653-5insCC MANE Select	ENSP00000303830.4:n.653-6_653-5insCC
ENST00000302850.9:c.653-6_653-5insCC	ENSP00000303830.4:n.653-6_653-5insCC
ENST00000341500.9:c.653-6_653-5insCC	ENSP00000342838.4:n.653-6_653-5insCC
ENST00000598216.1:n.628-6_628-5insCC
NM_000208.2:c.653-6_653-5insCC	NP_000199.2:n.653-6_653-5insCC
NM_000208.3:c.653-6_653-5insCC	NP_000199.2:n.653-6_653-5insCC
NM_001079817.1:c.653-6_653-5insCC	NP_001073285.1:n.653-6_653-5insCC
NM_001079817.2:c.653-6_653-5insCC	NP_001073285.1:n.653-6_653-5insCC
XM_011527988.1:c.731-6_731-5insCC	XP_011526290.1:n.731-6_731-5insCC
XM_011527989.1:c.731-6_731-5insCC	XP_011526291.1:n.731-6_731-5insCC
XM_011527988.2:c.653-6_653-5insCC	XP_011526290.2:n.653-6_653-5insCC
XM_011527989.3:c.653-6_653-5insCC	XP_011526291.2:n.653-6_653-5insCC
NM_000208.4:c.653-6_653-5insCC MANE Select	NP_000199.2:n.653-6_653-5insCC
NM_001079817.3:c.653-6_653-5insCC	NP_001073285.1:n.653-6_653-5insCC