Canonical Allele Identifier: CA304866863

Gene: INSR

Linked Data

• dbSNP Id: rs1024952676
• MyVariant Identifiers: chr19:g.7184671_7184686del (hg19) ; chr19:g.7184660_7184675del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184661_7184676del , CM000681.2:g.7184661_7184676del	GRCh38
NC_000019.9:g.7184672_7184687del , CM000681.1:g.7184672_7184687del	GRCh37
NC_000019.8:g.7135672_7135687del	NCBI36
NG_008852.2:g.114326_114341del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-38_653-23del MANE Select	ENSP00000303830.4:n.653-38_653-23del
ENST00000302850.9:c.653-38_653-23del	ENSP00000303830.4:n.653-38_653-23del
ENST00000341500.9:c.653-38_653-23del	ENSP00000342838.4:n.653-38_653-23del
ENST00000598216.1:n.628-38_628-23del
NM_000208.2:c.653-38_653-23del	NP_000199.2:n.653-38_653-23del
NM_000208.3:c.653-38_653-23del	NP_000199.2:n.653-38_653-23del
NM_001079817.1:c.653-38_653-23del	NP_001073285.1:n.653-38_653-23del
NM_001079817.2:c.653-38_653-23del	NP_001073285.1:n.653-38_653-23del
XM_011527988.1:c.731-38_731-23del	XP_011526290.1:n.731-38_731-23del
XM_011527989.1:c.731-38_731-23del	XP_011526291.1:n.731-38_731-23del
XM_011527988.2:c.653-38_653-23del	XP_011526290.2:n.653-38_653-23del
XM_011527989.3:c.653-38_653-23del	XP_011526291.2:n.653-38_653-23del
NM_000208.4:c.653-38_653-23del MANE Select	NP_000199.2:n.653-38_653-23del
NM_001079817.3:c.653-38_653-23del	NP_001073285.1:n.653-38_653-23del