Canonical Allele Identifier: CA2320763723

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117248C= , CM000681.2:g.7117248C=	GRCh38
NC_000019.9:g.7117259C= , CM000681.1:g.7117259C=	GRCh37
NC_000019.8:g.7068259C=	NCBI36
NG_008852.2:g.181753G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3957G= MANE Select	ENSP00000303830.4:p.Met1319=
ENST00000302850.9:c.3957G=	ENSP00000303830.4:p.Met1319=
ENST00000341500.9:c.3921G=	ENSP00000342838.4:p.Met1307=
NM_000208.2:c.3957G=	NP_000199.2:p.Met1319=
NM_000208.3:c.3957G=	NP_000199.2:p.Met1319=
NM_001079817.1:c.3921G=	NP_001073285.1:p.Met1307=
NM_001079817.2:c.3921G=	NP_001073285.1:p.Met1307=
XM_011527988.1:c.4032G=	XP_011526290.1:p.Met1344=
XM_011527989.1:c.3996G=	XP_011526291.1:p.Met1332=
XM_011527988.2:c.3954G=	XP_011526290.2:p.Met1318=
XM_011527989.3:c.3918G=	XP_011526291.2:p.Met1306=
NM_000208.4:c.3957G= MANE Select	NP_000199.2:p.Met1319=
NM_001079817.3:c.3921G=	NP_001073285.1:p.Met1307=