Canonical Allele Identifier: CA2320779430

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7150332A= , CM000681.2:g.7150332A=	GRCh38
NC_000019.9:g.7150343A= , CM000681.1:g.7150343A=	GRCh37
NC_000019.8:g.7101343A=	NCBI36
NG_008852.2:g.148669T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2267+165T= MANE Select	ENSP00000303830.4:n.2267+165T=
ENST00000302850.9:c.2267+165T=	ENSP00000303830.4:n.2267+165T=
ENST00000341500.9:c.2231+2394T=	ENSP00000342838.4:n.2231+2394T=
NM_000208.2:c.2267+165T=	NP_000199.2:n.2267+165T=
NM_000208.3:c.2267+165T=	NP_000199.2:n.2267+165T=
NM_001079817.1:c.2231+2394T=	NP_001073285.1:n.2231+2394T=
NM_001079817.2:c.2231+2394T=	NP_001073285.1:n.2231+2394T=
XM_011527988.1:c.2345+165T=	XP_011526290.1:n.2345+165T=
XM_011527989.1:c.2309+2394T=	XP_011526291.1:n.2309+2394T=
XM_011527988.2:c.2267+165T=	XP_011526290.2:n.2267+165T=
XM_011527989.3:c.2231+2394T=	XP_011526291.2:n.2231+2394T=
NM_000208.4:c.2267+165T= MANE Select	NP_000199.2:n.2267+165T=
NM_001079817.3:c.2231+2394T=	NP_001073285.1:n.2231+2394T=