Canonical Allele Identifier: CA403671370
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7125473A>C , CM000681.2:g.7125473A>C GRCh38
NC_000019.9:g.7125484A>C , CM000681.1:g.7125484A>C GRCh37
NC_000019.8:g.7076484A>C NCBI36
NG_008852.2:g.173528T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3068T>G MANE Select ENSP00000303830.4:p.Ile1023Ser
ENST00000302850.9:c.3068T>G ENSP00000303830.4:p.Ile1023Ser
ENST00000341500.9:c.3032T>G ENSP00000342838.4:p.Ile1011Ser
NM_000208.2:c.3068T>G NP_000199.2:p.Ile1023Ser
NM_000208.3:c.3068T>G NP_000199.2:p.Ile1023Ser
NM_001079817.1:c.3032T>G NP_001073285.1:p.Ile1011Ser
NM_001079817.2:c.3032T>G NP_001073285.1:p.Ile1011Ser
XM_011527988.1:c.3143T>G XP_011526290.1:p.Ile1048Ser
XM_011527989.1:c.3107T>G XP_011526291.1:p.Ile1036Ser
XM_011527988.2:c.3065T>G XP_011526290.2:p.Ile1022Ser
XM_011527989.3:c.3029T>G XP_011526291.2:p.Ile1010Ser
NM_000208.4:c.3068T>G MANE Select NP_000199.2:p.Ile1023Ser
NM_001079817.3:c.3032T>G NP_001073285.1:p.Ile1011Ser