Canonical Allele Identifier: CA2320836529

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7267748C= , CM000681.2:g.7267748C=	GRCh38
NC_000019.9:g.7267759C= , CM000681.1:g.7267759C=	GRCh37
NC_000019.8:g.7218759C=	NCBI36
NG_008852.2:g.31253G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.249G= MANE Select	ENSP00000303830.4:p.Met83=
ENST00000302850.9:c.249G=	ENSP00000303830.4:p.Met83=
ENST00000341500.9:c.249G=	ENSP00000342838.4:p.Met83=
ENST00000598216.1:n.224G=
NM_000208.2:c.249G=	NP_000199.2:p.Met83=
NM_000208.3:c.249G=	NP_000199.2:p.Met83=
NM_001079817.1:c.249G=	NP_001073285.1:p.Met83=
NM_001079817.2:c.249G=	NP_001073285.1:p.Met83=
XM_011527988.1:c.327G=	XP_011526290.1:p.Met109=
XM_011527989.1:c.327G=	XP_011526291.1:p.Met109=
XM_011527988.2:c.249G=	XP_011526290.2:p.Met83=
XM_011527989.3:c.249G=	XP_011526291.2:p.Met83=
NM_000208.4:c.249G= MANE Select	NP_000199.2:p.Met83=
NM_001079817.3:c.249G=	NP_001073285.1:p.Met83=