Canonical Allele Identifier: CA657053971

Gene: INSR

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117040_7117041insA , CM000681.2:g.7117040_7117041insA	GRCh38
NC_000019.9:g.7117051_7117052insA , CM000681.1:g.7117051_7117052insA	GRCh37
NC_000019.8:g.7068051_7068052insA	NCBI36
NG_008852.2:g.181960_181961insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.*15_*16insT MANE Select	ENSP00000303830.4:n.*15_*16insT
ENST00000302850.9:c.*15_*16insT	ENSP00000303830.4:n.*15_*16insT
ENST00000341500.9:c.*15_*16insT	ENSP00000342838.4:n.*15_*16insT
NM_000208.2:c.*15_*16insT	NP_000199.2:n.*15_*16insT
NM_000208.3:c.*15_*16insT	NP_000199.2:n.*15_*16insT
NM_001079817.1:c.*15_*16insT	NP_001073285.1:n.*15_*16insT
NM_001079817.2:c.*15_*16insT	NP_001073285.1:n.*15_*16insT
XM_011527988.1:c.*15_*16insT	XP_011526290.1:n.*15_*16insT
XM_011527989.1:c.*15_*16insT	XP_011526291.1:n.*15_*16insT
XM_011527988.2:c.*15_*16insT	XP_011526290.2:n.*15_*16insT
XM_011527989.3:c.*15_*16insT	XP_011526291.2:n.*15_*16insT
NM_000208.4:c.*15_*16insT MANE Select	NP_000199.2:n.*15_*16insT
NM_001079817.3:c.*15_*16insT	NP_001073285.1:n.*15_*16insT