Canonical Allele Identifier: CA2320763713

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117222G= , CM000681.2:g.7117222G=	GRCh38
NC_000019.9:g.7117233G= , CM000681.1:g.7117233G=	GRCh37
NC_000019.8:g.7068233G=	NCBI36
NG_008852.2:g.181779C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3983C= MANE Select	ENSP00000303830.4:p.Pro1328=
ENST00000302850.9:c.3983C=	ENSP00000303830.4:p.Pro1328=
ENST00000341500.9:c.3947C=	ENSP00000342838.4:p.Pro1316=
NM_000208.2:c.3983C=	NP_000199.2:p.Pro1328=
NM_000208.3:c.3983C=	NP_000199.2:p.Pro1328=
NM_001079817.1:c.3947C=	NP_001073285.1:p.Pro1316=
NM_001079817.2:c.3947C=	NP_001073285.1:p.Pro1316=
XM_011527988.1:c.4058C=	XP_011526290.1:p.Pro1353=
XM_011527989.1:c.4022C=	XP_011526291.1:p.Pro1341=
XM_011527988.2:c.3980C=	XP_011526290.2:p.Pro1327=
XM_011527989.3:c.3944C=	XP_011526291.2:p.Pro1315=
NM_000208.4:c.3983C= MANE Select	NP_000199.2:p.Pro1328=
NM_001079817.3:c.3947C=	NP_001073285.1:p.Pro1316=