Canonical Allele Identifier: CA403669577
Gene: INSR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7120750C>G (hg19) chr19:g.7120739C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7120739C>G , CM000681.2:g.7120739C>G GRCh38
NC_000019.9:g.7120750C>G , CM000681.1:g.7120750C>G GRCh37
NC_000019.8:g.7071750C>G NCBI36
NG_008852.2:g.178262G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.3540G>C MANE Select ENSP00000303830.4:p.Met1180Ile
ENST00000302850.9:c.3540G>C ENSP00000303830.4:p.Met1180Ile
ENST00000341500.9:c.3504G>C ENSP00000342838.4:p.Met1168Ile
ENST00000601099.1:n.451G>C
NM_000208.2:c.3540G>C NP_000199.2:p.Met1180Ile
NM_000208.3:c.3540G>C NP_000199.2:p.Met1180Ile
NM_001079817.1:c.3504G>C NP_001073285.1:p.Met1168Ile
NM_001079817.2:c.3504G>C NP_001073285.1:p.Met1168Ile
XM_011527988.1:c.3615G>C XP_011526290.1:p.Met1205Ile
XM_011527989.1:c.3579G>C XP_011526291.1:p.Met1193Ile
XM_011527988.2:c.3537G>C XP_011526290.2:p.Met1179Ile
XM_011527989.3:c.3501G>C XP_011526291.2:p.Met1167Ile
NM_000208.4:c.3540G>C MANE Select NP_000199.2:p.Met1180Ile
NM_001079817.3:c.3504G>C NP_001073285.1:p.Met1168Ile
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