Canonical Allele Identifier: CA403668561
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117229T>C , CM000681.2:g.7117229T>C GRCh38
NC_000019.9:g.7117240T>C , CM000681.1:g.7117240T>C GRCh37
NC_000019.8:g.7068240T>C NCBI36
NG_008852.2:g.181772A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3976A>G MANE Select ENSP00000303830.4:p.Asn1326Asp
ENST00000302850.9:c.3976A>G ENSP00000303830.4:p.Asn1326Asp
ENST00000341500.9:c.3940A>G ENSP00000342838.4:p.Asn1314Asp
NM_000208.2:c.3976A>G NP_000199.2:p.Asn1326Asp
NM_000208.3:c.3976A>G NP_000199.2:p.Asn1326Asp
NM_001079817.1:c.3940A>G NP_001073285.1:p.Asn1314Asp
NM_001079817.2:c.3940A>G NP_001073285.1:p.Asn1314Asp
XM_011527988.1:c.4051A>G XP_011526290.1:p.Asn1351Asp
XM_011527989.1:c.4015A>G XP_011526291.1:p.Asn1339Asp
XM_011527988.2:c.3973A>G XP_011526290.2:p.Asn1325Asp
XM_011527989.3:c.3937A>G XP_011526291.2:p.Asn1313Asp
NM_000208.4:c.3976A>G MANE Select NP_000199.2:p.Asn1326Asp
NM_001079817.3:c.3940A>G NP_001073285.1:p.Asn1314Asp