Canonical Allele Identifier: CA124259
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 14705
ClinVar RCV Id: RCV000015820
dbSNP Id: rs121913155
MyVariant Identifiers: chr19:g.7267566T>A (hg19) chr19:g.7267555T>A (hg38)
PubMed: PMID:8101305 PMID:27896077
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7267555T>A , CM000681.2:g.7267555T>A GRCh38
NC_000019.9:g.7267566T>A , CM000681.1:g.7267566T>A GRCh37
NC_000019.8:g.7218566T>A NCBI36
NG_008852.2:g.31446A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.442A>T MANE Select ENSP00000303830.4:p.Lys148Ter
ENST00000302850.9:c.442A>T ENSP00000303830.4:p.Lys148Ter
ENST00000341500.9:c.442A>T ENSP00000342838.4:p.Lys148Ter
ENST00000598216.1:n.417A>T
NM_000208.2:c.442A>T NP_000199.2:p.Lys148Ter
NM_000208.3:c.442A>T NP_000199.2:p.Lys148Ter
NM_001079817.1:c.442A>T NP_001073285.1:p.Lys148Ter
NM_001079817.2:c.442A>T NP_001073285.1:p.Lys148Ter
XM_011527988.1:c.520A>T XP_011526290.1:p.Lys174Ter
XM_011527989.1:c.520A>T XP_011526291.1:p.Lys174Ter
XM_011527988.2:c.442A>T XP_011526290.2:p.Lys148Ter
XM_011527989.3:c.442A>T XP_011526291.2:p.Lys148Ter
NM_000208.4:c.442A>T MANE Select NP_000199.2:p.Lys148Ter
NM_001079817.3:c.442A>T NP_001073285.1:p.Lys148Ter
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