Canonical Allele Identifier: CA631723717

Gene: INSR

Linked Data

• dbSNP Id: rs1568470677
• gnomAD v2: 19-7184669-A-AGAGG
• MyVariant Identifiers: chr19:g.7184669_7184670insGAGG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184661_7184664dup , CM000681.2:g.7184661_7184664dup	GRCh38
NC_000019.9:g.7184672_7184675dup , CM000681.1:g.7184672_7184675dup	GRCh37
NC_000019.8:g.7135672_7135675dup	NCBI36
NG_008852.2:g.114339_114342dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-25_653-22dup MANE Select	ENSP00000303830.4:n.653-25_653-22dup
ENST00000302850.9:c.653-25_653-22dup	ENSP00000303830.4:n.653-25_653-22dup
ENST00000341500.9:c.653-25_653-22dup	ENSP00000342838.4:n.653-25_653-22dup
ENST00000598216.1:n.628-25_628-22dup
NM_000208.2:c.653-25_653-22dup	NP_000199.2:n.653-25_653-22dup
NM_000208.3:c.653-25_653-22dup	NP_000199.2:n.653-25_653-22dup
NM_001079817.1:c.653-25_653-22dup	NP_001073285.1:n.653-25_653-22dup
NM_001079817.2:c.653-25_653-22dup	NP_001073285.1:n.653-25_653-22dup
XM_011527988.1:c.731-25_731-22dup	XP_011526290.1:n.731-25_731-22dup
XM_011527989.1:c.731-25_731-22dup	XP_011526291.1:n.731-25_731-22dup
XM_011527988.2:c.653-25_653-22dup	XP_011526290.2:n.653-25_653-22dup
XM_011527989.3:c.653-25_653-22dup	XP_011526291.2:n.653-25_653-22dup
NM_000208.4:c.653-25_653-22dup MANE Select	NP_000199.2:n.653-25_653-22dup
NM_001079817.3:c.653-25_653-22dup	NP_001073285.1:n.653-25_653-22dup