Canonical Allele Identifier: CA9135455
Gene: INSR HGNC NCBI

Linked Data

dbSNP Id: rs387906538
gnomAD v3: 19-7132230-G-C
gnomAD v4: 19-7132230-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7132230G>C , CM000681.2:g.7132230G>C GRCh38
NC_000019.9:g.7132241G>C , CM000681.1:g.7132241G>C GRCh37
NC_000019.8:g.7083241G>C NCBI36
NG_008852.2:g.166771C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.2770C>G MANE Select ENSP00000303830.4:p.Arg924Gly
ENST00000302850.9:c.2770C>G ENSP00000303830.4:p.Arg924Gly
ENST00000341500.9:c.2734C>G ENSP00000342838.4:p.Arg912Gly
NM_000208.2:c.2770C>G NP_000199.2:p.Arg924Gly
NM_000208.3:c.2770C>G NP_000199.2:p.Arg924Gly
NM_001079817.1:c.2734C>G NP_001073285.1:p.Arg912Gly
NM_001079817.2:c.2734C>G NP_001073285.1:p.Arg912Gly
XM_011527988.1:c.2848C>G XP_011526290.1:p.Arg950Gly
XM_011527989.1:c.2812C>G XP_011526291.1:p.Arg938Gly
XM_011527988.2:c.2770C>G XP_011526290.2:p.Arg924Gly
XM_011527989.3:c.2734C>G XP_011526291.2:p.Arg912Gly
NM_000208.4:c.2770C>G MANE Select NP_000199.2:p.Arg924Gly
NM_001079817.3:c.2734C>G NP_001073285.1:p.Arg912Gly