Canonical Allele Identifier: CA631692594

Gene: INSR

Linked Data

• dbSNP Id: rs1182364580
• gnomAD v2: 19-7119572-CCCAAAGGACCACG-C
• MyVariant Identifiers: chr19:g.7119573_7119585del (hg19) ; chr19:g.7119562_7119574del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7119572_7119584del , CM000681.2:g.7119572_7119584del	GRCh38
NC_000019.9:g.7119583_7119595del , CM000681.1:g.7119583_7119595del	GRCh37
NC_000019.8:g.7070583_7070595del	NCBI36
NG_008852.2:g.179427_179439del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3669_3681del
ENST00000302850.9:c.3669_3681del
ENST00000341500.9:c.3633_3645del
NM_000208.2:c.3669_3681del
NM_000208.3:c.3669_3681del
NM_001079817.1:c.3633_3645del
NM_001079817.2:c.3633_3645del
XM_011527988.1:c.3744_3756del
XM_011527989.1:c.3708_3720del
XM_011527988.2:c.3666_3678del
XM_011527989.3:c.3630_3642del
NM_000208.4:c.3669_3681del
NM_001079817.3:c.3633_3645del