Canonical Allele Identifier: CA2320765487
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7120587C= , CM000681.2:g.7120587C= GRCh38
NC_000019.9:g.7120598C= , CM000681.1:g.7120598C= GRCh37
NC_000019.8:g.7071598C= NCBI36
NG_008852.2:g.178414G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3659+33G= MANE Select ENSP00000303830.4:n.3659+33G=
ENST00000302850.9:c.3659+33G= ENSP00000303830.4:n.3659+33G=
ENST00000341500.9:c.3623+33G= ENSP00000342838.4:n.3623+33G=
NM_000208.2:c.3659+33G= NP_000199.2:n.3659+33G=
NM_000208.3:c.3659+33G= NP_000199.2:n.3659+33G=
NM_001079817.1:c.3623+33G= NP_001073285.1:n.3623+33G=
NM_001079817.2:c.3623+33G= NP_001073285.1:n.3623+33G=
XM_011527988.1:c.3734+33G= XP_011526290.1:n.3734+33G=
XM_011527989.1:c.3698+33G= XP_011526291.1:n.3698+33G=
XM_011527988.2:c.3656+33G= XP_011526290.2:n.3656+33G=
XM_011527989.3:c.3620+33G= XP_011526291.2:n.3620+33G=
NM_000208.4:c.3659+33G= MANE Select NP_000199.2:n.3659+33G=
NM_001079817.3:c.3623+33G= NP_001073285.1:n.3623+33G=