Canonical Allele Identifier: CA631723727

Gene: INSR

Linked Data

• dbSNP Id: rs1311305315
• gnomAD v2: 19-7184679-AAATAAAT-A
• gnomAD v4: 19-7184668-AAATAAAT-A
• MyVariant Identifiers: chr19:g.7184680_7184686del (hg19) ; chr19:g.7184669_7184675del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184671_7184677del , CM000681.2:g.7184671_7184677del	GRCh38
NC_000019.9:g.7184682_7184688del , CM000681.1:g.7184682_7184688del	GRCh37
NC_000019.8:g.7135682_7135688del	NCBI36
NG_008852.2:g.114326_114332del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-38_653-32del MANE Select	ENSP00000303830.4:n.653-38_653-32del
ENST00000302850.9:c.653-38_653-32del	ENSP00000303830.4:n.653-38_653-32del
ENST00000341500.9:c.653-38_653-32del	ENSP00000342838.4:n.653-38_653-32del
ENST00000598216.1:n.628-38_628-32del
NM_000208.2:c.653-38_653-32del	NP_000199.2:n.653-38_653-32del
NM_000208.3:c.653-38_653-32del	NP_000199.2:n.653-38_653-32del
NM_001079817.1:c.653-38_653-32del	NP_001073285.1:n.653-38_653-32del
NM_001079817.2:c.653-38_653-32del	NP_001073285.1:n.653-38_653-32del
XM_011527988.1:c.731-38_731-32del	XP_011526290.1:n.731-38_731-32del
XM_011527989.1:c.731-38_731-32del	XP_011526291.1:n.731-38_731-32del
XM_011527988.2:c.653-38_653-32del	XP_011526290.2:n.653-38_653-32del
XM_011527989.3:c.653-38_653-32del	XP_011526291.2:n.653-38_653-32del
NM_000208.4:c.653-38_653-32del MANE Select	NP_000199.2:n.653-38_653-32del
NM_001079817.3:c.653-38_653-32del	NP_001073285.1:n.653-38_653-32del