Canonical Allele Identifier: CA2320765546

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120739C= , CM000681.2:g.7120739C=	GRCh38
NC_000019.9:g.7120750C= , CM000681.1:g.7120750C=	GRCh37
NC_000019.8:g.7071750C=	NCBI36
NG_008852.2:g.178262G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000208.4:c.3540G= MANE Select	NP_000199.2:p.Met1180=
ENST00000302850.10:c.3540G= MANE Select	ENSP00000303830.4:p.Met1180=
NM_000208.2:c.3540G=	NP_000199.2:p.Met1180=
NM_000208.3:c.3540G=	NP_000199.2:p.Met1180=
NM_001079817.1:c.3504G=	NP_001073285.1:p.Met1168=
NM_001079817.2:c.3504G=	NP_001073285.1:p.Met1168=
NM_001079817.3:c.3504G=	NP_001073285.1:p.Met1168=
ENST00000302850.9:c.3540G=	ENSP00000303830.4:p.Met1180=
ENST00000341500.9:c.3504G=	ENSP00000342838.4:p.Met1168=
ENST00000601099.1:n.451G=
XM_011527988.1:c.3615G=	XP_011526290.1:p.Met1205=
XM_011527988.2:c.3537G=	XP_011526290.2:p.Met1179=
XM_011527989.1:c.3579G=	XP_011526291.1:p.Met1193=
XM_011527989.3:c.3501G=	XP_011526291.2:p.Met1167=