Canonical Allele Identifier: CA505216534

Gene: INSR

Linked Data

• dbSNP Id: rs1555734569
• MyVariant Identifiers: chr19:g.7119588_7119593del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7119577_7119582del , CM000681.2:g.7119577_7119582del	GRCh38
NC_000019.9:g.7119588_7119593del , CM000681.1:g.7119588_7119593del	GRCh37
NC_000019.8:g.7070588_7070593del	NCBI36
NG_008852.2:g.179419_179424del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3661_3666del MANE Select	ENSP00000303830.4:p.Ser1221_Phe1222del
ENST00000302850.9:c.3661_3666del	ENSP00000303830.4:p.Ser1221_Phe1222del
ENST00000341500.9:c.3625_3630del	ENSP00000342838.4:p.Ser1209_Phe1210del
NM_000208.2:c.3661_3666del	NP_000199.2:p.Ser1221_Phe1222del
NM_000208.3:c.3661_3666del	NP_000199.2:p.Ser1221_Phe1222del
NM_001079817.1:c.3625_3630del	NP_001073285.1:p.Ser1209_Phe1210del
NM_001079817.2:c.3625_3630del	NP_001073285.1:p.Ser1209_Phe1210del
XM_011527988.1:c.3736_3741del	XP_011526290.1:p.Ser1246_Phe1247del
XM_011527989.1:c.3700_3705del	XP_011526291.1:p.Ser1234_Phe1235del
XM_011527988.2:c.3658_3663del	XP_011526290.2:p.Ser1220_Phe1221del
XM_011527989.3:c.3622_3627del	XP_011526291.2:p.Ser1208_Phe1209del
NM_000208.4:c.3661_3666del MANE Select	NP_000199.2:p.Ser1221_Phe1222del
NM_001079817.3:c.3625_3630del	NP_001073285.1:p.Ser1209_Phe1210del