Canonical Allele Identifier: CA2320761564

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7112257T= , CM000681.2:g.7112257T=	GRCh38
NC_000019.9:g.7112268T= , CM000681.1:g.7112268T=	GRCh37
NC_000019.8:g.7063268T=	NCBI36
NG_008852.2:g.186744A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341500.9:c.*4799A=	ENSP00000342838.4:n.*4799A=
NM_000208.2:c.*4799A=	NP_000199.2:n.*4799A=
NM_000208.3:c.*4799A=	NP_000199.2:n.*4799A=
NM_001079817.1:c.*4799A=	NP_001073285.1:n.*4799A=
NM_001079817.2:c.*4799A=	NP_001073285.1:n.*4799A=
XM_011527988.2:c.*4799A=	XP_011526290.2:n.*4799A=
XM_011527989.3:c.*4799A=	XP_011526291.2:n.*4799A=