Canonical Allele Identifier: CA2320790738

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7172383G= , CM000681.2:g.7172383G=	GRCh38
NC_000019.9:g.7172394G= , CM000681.1:g.7172394G=	GRCh37
NC_000019.8:g.7123394G=	NCBI36
NG_008852.2:g.126618C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.1175C= MANE Select	ENSP00000303830.4:p.Ser392=
ENST00000302850.9:c.1175C=	ENSP00000303830.4:p.Ser392=
ENST00000341500.9:c.1175C=	ENSP00000342838.4:p.Ser392=
ENST00000598216.1:n.1150C=
NM_000208.2:c.1175C=	NP_000199.2:p.Ser392=
NM_000208.3:c.1175C=	NP_000199.2:p.Ser392=
NM_001079817.1:c.1175C=	NP_001073285.1:p.Ser392=
NM_001079817.2:c.1175C=	NP_001073285.1:p.Ser392=
XM_011527988.1:c.1253C=	XP_011526290.1:p.Ser418=
XM_011527989.1:c.1253C=	XP_011526291.1:p.Ser418=
XM_011527988.2:c.1175C=	XP_011526290.2:p.Ser392=
XM_011527989.3:c.1175C=	XP_011526291.2:p.Ser392=
NM_000208.4:c.1175C= MANE Select	NP_000199.2:p.Ser392=
NM_001079817.3:c.1175C=	NP_001073285.1:p.Ser392=