Canonical Allele Identifier: CA2320763994

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117081G= , CM000681.2:g.7117081G=	GRCh38
NC_000019.9:g.7117092G= , CM000681.1:g.7117092G=	GRCh37
NC_000019.8:g.7068092G=	NCBI36
NG_008852.2:g.181920C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4124C= MANE Select	ENSP00000303830.4:p.Thr1375=
ENST00000302850.9:c.4124C=	ENSP00000303830.4:p.Thr1375=
ENST00000341500.9:c.4088C=	ENSP00000342838.4:p.Thr1363=
NM_000208.2:c.4124C=	NP_000199.2:p.Thr1375=
NM_000208.3:c.4124C=	NP_000199.2:p.Thr1375=
NM_001079817.1:c.4088C=	NP_001073285.1:p.Thr1363=
NM_001079817.2:c.4088C=	NP_001073285.1:p.Thr1363=
XM_011527988.1:c.4199C=	XP_011526290.1:p.Thr1400=
XM_011527989.1:c.4163C=	XP_011526291.1:p.Thr1388=
XM_011527988.2:c.4121C=	XP_011526290.2:p.Thr1374=
XM_011527989.3:c.4085C=	XP_011526291.2:p.Thr1362=
NM_000208.4:c.4124C= MANE Select	NP_000199.2:p.Thr1375=
NM_001079817.3:c.4088C=	NP_001073285.1:p.Thr1363=