Canonical Allele Identifier: CA2320768119

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125733A= , CM000681.2:g.7125733A=	GRCh38
NC_000019.9:g.7125744A= , CM000681.1:g.7125744A=	GRCh37
NC_000019.8:g.7076744A=	NCBI36
NG_008852.2:g.173268T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3014-206T= MANE Select	ENSP00000303830.4:n.3014-206T=
ENST00000302850.9:c.3014-206T=	ENSP00000303830.4:n.3014-206T=
ENST00000341500.9:c.2978-206T=	ENSP00000342838.4:n.2978-206T=
NM_000208.2:c.3014-206T=	NP_000199.2:n.3014-206T=
NM_000208.3:c.3014-206T=	NP_000199.2:n.3014-206T=
NM_001079817.1:c.2978-206T=	NP_001073285.1:n.2978-206T=
NM_001079817.2:c.2978-206T=	NP_001073285.1:n.2978-206T=
XM_011527988.1:c.3089-206T=	XP_011526290.1:n.3089-206T=
XM_011527989.1:c.3053-206T=	XP_011526291.1:n.3053-206T=
XM_011527988.2:c.3011-206T=	XP_011526290.2:n.3011-206T=
XM_011527989.3:c.2975-206T=	XP_011526291.2:n.2975-206T=
NM_000208.4:c.3014-206T= MANE Select	NP_000199.2:n.3014-206T=
NM_001079817.3:c.2978-206T=	NP_001073285.1:n.2978-206T=