Canonical Allele Identifier: CA403671013
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7125305T>A , CM000681.2:g.7125305T>A GRCh38
NC_000019.9:g.7125316T>A , CM000681.1:g.7125316T>A GRCh37
NC_000019.8:g.7076316T>A NCBI36
NG_008852.2:g.173696A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3236A>T MANE Select ENSP00000303830.4:p.Lys1079Met
ENST00000302850.9:c.3236A>T ENSP00000303830.4:p.Lys1079Met
ENST00000341500.9:c.3200A>T ENSP00000342838.4:p.Lys1067Met
ENST00000593970.1:n.82A>T
NM_000208.2:c.3236A>T NP_000199.2:p.Lys1079Met
NM_000208.3:c.3236A>T NP_000199.2:p.Lys1079Met
NM_001079817.1:c.3200A>T NP_001073285.1:p.Lys1067Met
NM_001079817.2:c.3200A>T NP_001073285.1:p.Lys1067Met
XM_011527988.1:c.3311A>T XP_011526290.1:p.Lys1104Met
XM_011527989.1:c.3275A>T XP_011526291.1:p.Lys1092Met
XM_011527988.2:c.3233A>T XP_011526290.2:p.Lys1078Met
XM_011527989.3:c.3197A>T XP_011526291.2:p.Lys1066Met
NM_000208.4:c.3236A>T MANE Select NP_000199.2:p.Lys1079Met
NM_001079817.3:c.3200A>T NP_001073285.1:p.Lys1067Met