Canonical Allele Identifier: CA2320767912

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125313C= , CM000681.2:g.7125313C=	GRCh38
NC_000019.9:g.7125324C= , CM000681.1:g.7125324C=	GRCh37
NC_000019.8:g.7076324C=	NCBI36
NG_008852.2:g.173688G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3228G= MANE Select	ENSP00000303830.4:p.Ser1076=
ENST00000302850.9:c.3228G=	ENSP00000303830.4:p.Ser1076=
ENST00000341500.9:c.3192G=	ENSP00000342838.4:p.Ser1064=
ENST00000593970.1:n.74G=
NM_000208.2:c.3228G=	NP_000199.2:p.Ser1076=
NM_000208.3:c.3228G=	NP_000199.2:p.Ser1076=
NM_001079817.1:c.3192G=	NP_001073285.1:p.Ser1064=
NM_001079817.2:c.3192G=	NP_001073285.1:p.Ser1064=
XM_011527988.1:c.3303G=	XP_011526290.1:p.Ser1101=
XM_011527989.1:c.3267G=	XP_011526291.1:p.Ser1089=
XM_011527988.2:c.3225G=	XP_011526290.2:p.Ser1075=
XM_011527989.3:c.3189G=	XP_011526291.2:p.Ser1063=
NM_000208.4:c.3228G= MANE Select	NP_000199.2:p.Ser1076=
NM_001079817.3:c.3192G=	NP_001073285.1:p.Ser1064=