Canonical Allele Identifier: CA2320779428

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7150329C= , CM000681.2:g.7150329C=	GRCh38
NC_000019.9:g.7150340C= , CM000681.1:g.7150340C=	GRCh37
NC_000019.8:g.7101340C=	NCBI36
NG_008852.2:g.148672G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2267+168G= MANE Select	ENSP00000303830.4:n.2267+168G=
ENST00000302850.9:c.2267+168G=	ENSP00000303830.4:n.2267+168G=
ENST00000341500.9:c.2231+2397G=	ENSP00000342838.4:n.2231+2397G=
NM_000208.2:c.2267+168G=	NP_000199.2:n.2267+168G=
NM_000208.3:c.2267+168G=	NP_000199.2:n.2267+168G=
NM_001079817.1:c.2231+2397G=	NP_001073285.1:n.2231+2397G=
NM_001079817.2:c.2231+2397G=	NP_001073285.1:n.2231+2397G=
XM_011527988.1:c.2345+168G=	XP_011526290.1:n.2345+168G=
XM_011527989.1:c.2309+2397G=	XP_011526291.1:n.2309+2397G=
XM_011527988.2:c.2267+168G=	XP_011526290.2:n.2267+168G=
XM_011527989.3:c.2231+2397G=	XP_011526291.2:n.2231+2397G=
NM_000208.4:c.2267+168G= MANE Select	NP_000199.2:n.2267+168G=
NM_001079817.3:c.2231+2397G=	NP_001073285.1:n.2231+2397G=