Canonical Allele Identifier: CA2320771078

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132234G= , CM000681.2:g.7132234G=	GRCh38
NC_000019.9:g.7132245G= , CM000681.1:g.7132245G=	GRCh37
NC_000019.8:g.7083245G=	NCBI36
NG_008852.2:g.166767C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2766C= MANE Select	ENSP00000303830.4:p.Ser922=
ENST00000302850.9:c.2766C=	ENSP00000303830.4:p.Ser922=
ENST00000341500.9:c.2730C=	ENSP00000342838.4:p.Ser910=
NM_000208.2:c.2766C=	NP_000199.2:p.Ser922=
NM_000208.3:c.2766C=	NP_000199.2:p.Ser922=
NM_001079817.1:c.2730C=	NP_001073285.1:p.Ser910=
NM_001079817.2:c.2730C=	NP_001073285.1:p.Ser910=
XM_011527988.1:c.2844C=	XP_011526290.1:p.Ser948=
XM_011527989.1:c.2808C=	XP_011526291.1:p.Ser936=
XM_011527988.2:c.2766C=	XP_011526290.2:p.Ser922=
XM_011527989.3:c.2730C=	XP_011526291.2:p.Ser910=
NM_000208.4:c.2766C= MANE Select	NP_000199.2:p.Ser922=
NM_001079817.3:c.2730C=	NP_001073285.1:p.Ser910=