Canonical Allele Identifier: CA2320780980
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7152688T= , CM000681.2:g.7152688T= GRCh38
NC_000019.9:g.7152699T= , CM000681.1:g.7152699T= GRCh37
NC_000019.8:g.7103699T= NCBI36
NG_008852.2:g.146313A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.2231+38A= MANE Select ENSP00000303830.4:n.2231+38A=
ENST00000302850.9:c.2231+38A= ENSP00000303830.4:n.2231+38A=
ENST00000341500.9:c.2231+38A= ENSP00000342838.4:n.2231+38A=
ENST00000598216.1:n.2244A=
NM_000208.2:c.2231+38A= NP_000199.2:n.2231+38A=
NM_000208.3:c.2231+38A= NP_000199.2:n.2231+38A=
NM_001079817.1:c.2231+38A= NP_001073285.1:n.2231+38A=
NM_001079817.2:c.2231+38A= NP_001073285.1:n.2231+38A=
XM_011527988.1:c.2309+38A= XP_011526290.1:n.2309+38A=
XM_011527989.1:c.2309+38A= XP_011526291.1:n.2309+38A=
XM_011527988.2:c.2231+38A= XP_011526290.2:n.2231+38A=
XM_011527989.3:c.2231+38A= XP_011526291.2:n.2231+38A=
NM_000208.4:c.2231+38A= MANE Select NP_000199.2:n.2231+38A=
NM_001079817.3:c.2231+38A= NP_001073285.1:n.2231+38A=