Canonical Allele Identifier: CA2320771062
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7132190G= , CM000681.2:g.7132190G= GRCh38
NC_000019.9:g.7132201G= , CM000681.1:g.7132201G= GRCh37
NC_000019.8:g.7083201G= NCBI36
NG_008852.2:g.166811C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.2810C= MANE Select ENSP00000303830.4:p.Thr937=
ENST00000302850.9:c.2810C= ENSP00000303830.4:p.Thr937=
ENST00000341500.9:c.2774C= ENSP00000342838.4:p.Thr925=
NM_000208.2:c.2810C= NP_000199.2:p.Thr937=
NM_000208.3:c.2810C= NP_000199.2:p.Thr937=
NM_001079817.1:c.2774C= NP_001073285.1:p.Thr925=
NM_001079817.2:c.2774C= NP_001073285.1:p.Thr925=
XM_011527988.1:c.2888C= XP_011526290.1:p.Thr963=
XM_011527989.1:c.2852C= XP_011526291.1:p.Thr951=
XM_011527988.2:c.2810C= XP_011526290.2:p.Thr937=
XM_011527989.3:c.2774C= XP_011526291.2:p.Thr925=
NM_000208.4:c.2810C= MANE Select NP_000199.2:p.Thr937=
NM_001079817.3:c.2774C= NP_001073285.1:p.Thr925=