Canonical Allele Identifier: CA124269
Gene: INSR HGNC NCBI

Linked Data

dbSNP Id: rs121913158
MyVariant Identifiers: chr19:g.7170715C>G (hg19) chr19:g.7170704C>G (hg38)
PubMed: PMID:8188715 PMID:27896077
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7170704C>G , CM000681.2:g.7170704C>G GRCh38
NC_000019.9:g.7170715C>G , CM000681.1:g.7170715C>G GRCh37
NC_000019.8:g.7121715C>G NCBI36
NG_008852.2:g.128297G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.1316G>C MANE Select ENSP00000303830.4:p.Trp439Ser
ENST00000302850.9:c.1316G>C ENSP00000303830.4:p.Trp439Ser
ENST00000341500.9:c.1316G>C ENSP00000342838.4:p.Trp439Ser
ENST00000598216.1:n.1291G>C
NM_000208.2:c.1316G>C NP_000199.2:p.Trp439Ser
NM_000208.3:c.1316G>C NP_000199.2:p.Trp439Ser
NM_001079817.1:c.1316G>C NP_001073285.1:p.Trp439Ser
NM_001079817.2:c.1316G>C NP_001073285.1:p.Trp439Ser
XM_011527988.1:c.1394G>C XP_011526290.1:p.Trp465Ser
XM_011527989.1:c.1394G>C XP_011526291.1:p.Trp465Ser
XM_011527988.2:c.1316G>C XP_011526290.2:p.Trp439Ser
XM_011527989.3:c.1316G>C XP_011526291.2:p.Trp439Ser
NM_000208.4:c.1316G>C MANE Select NP_000199.2:p.Trp439Ser
NM_001079817.3:c.1316G>C NP_001073285.1:p.Trp439Ser
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