Canonical Allele Identifier: CA2320776131

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7143068G= , CM000681.2:g.7143068G=	GRCh38
NC_000019.9:g.7143079G= , CM000681.1:g.7143079G=	GRCh37
NC_000019.8:g.7094079G=	NCBI36
NG_008852.2:g.155933C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2290C= MANE Select	ENSP00000303830.4:p.Leu764=
ENST00000302850.9:c.2290C=	ENSP00000303830.4:p.Leu764=
ENST00000341500.9:c.2254C=	ENSP00000342838.4:p.Leu752=
NM_000208.2:c.2290C=	NP_000199.2:p.Leu764=
NM_000208.3:c.2290C=	NP_000199.2:p.Leu764=
NM_001079817.1:c.2254C=	NP_001073285.1:p.Leu752=
NM_001079817.2:c.2254C=	NP_001073285.1:p.Leu752=
XM_011527988.1:c.2368C=	XP_011526290.1:p.Leu790=
XM_011527989.1:c.2332C=	XP_011526291.1:p.Leu778=
XM_011527988.2:c.2290C=	XP_011526290.2:p.Leu764=
XM_011527989.3:c.2254C=	XP_011526291.2:p.Leu752=
NM_000208.4:c.2290C= MANE Select	NP_000199.2:p.Leu764=
NM_001079817.3:c.2254C=	NP_001073285.1:p.Leu752=