Canonical Allele Identifier: CA403671179
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7125383C>A , CM000681.2:g.7125383C>A GRCh38
NC_000019.9:g.7125394C>A , CM000681.1:g.7125394C>A GRCh37
NC_000019.8:g.7076394C>A NCBI36
NG_008852.2:g.173618G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3158G>T MANE Select ENSP00000303830.4:p.Arg1053Leu
ENST00000302850.9:c.3158G>T ENSP00000303830.4:p.Arg1053Leu
ENST00000341500.9:c.3122G>T ENSP00000342838.4:p.Arg1041Leu
ENST00000593970.1:n.4G>T
NM_000208.2:c.3158G>T NP_000199.2:p.Arg1053Leu
NM_000208.3:c.3158G>T NP_000199.2:p.Arg1053Leu
NM_001079817.1:c.3122G>T NP_001073285.1:p.Arg1041Leu
NM_001079817.2:c.3122G>T NP_001073285.1:p.Arg1041Leu
XM_011527988.1:c.3233G>T XP_011526290.1:p.Arg1078Leu
XM_011527989.1:c.3197G>T XP_011526291.1:p.Arg1066Leu
XM_011527988.2:c.3155G>T XP_011526290.2:p.Arg1052Leu
XM_011527989.3:c.3119G>T XP_011526291.2:p.Arg1040Leu
NM_000208.4:c.3158G>T MANE Select NP_000199.2:p.Arg1053Leu
NM_001079817.3:c.3122G>T NP_001073285.1:p.Arg1041Leu