Canonical Allele Identifier: CA2320768001

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125527A= , CM000681.2:g.7125527A=	GRCh38
NC_000019.9:g.7125538A= , CM000681.1:g.7125538A=	GRCh37
NC_000019.8:g.7076538A=	NCBI36
NG_008852.2:g.173474T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3014T= MANE Select	ENSP00000303830.4:p.Val1005=
ENST00000302850.9:c.3014T=	ENSP00000303830.4:p.Val1005=
ENST00000341500.9:c.2978T=	ENSP00000342838.4:p.Val993=
NM_000208.2:c.3014T=	NP_000199.2:p.Val1005=
NM_000208.3:c.3014T=	NP_000199.2:p.Val1005=
NM_001079817.1:c.2978T=	NP_001073285.1:p.Val993=
NM_001079817.2:c.2978T=	NP_001073285.1:p.Val993=
XM_011527988.1:c.3089T=	XP_011526290.1:p.Val1030=
XM_011527989.1:c.3053T=	XP_011526291.1:p.Val1018=
XM_011527988.2:c.3011T=	XP_011526290.2:p.Val1004=
XM_011527989.3:c.2975T=	XP_011526291.2:p.Val992=
NM_000208.4:c.3014T= MANE Select	NP_000199.2:p.Val1005=
NM_001079817.3:c.2978T=	NP_001073285.1:p.Val993=