Canonical Allele Identifier: CA403664612

Gene: INSR

Linked Data

• dbSNP Id: rs1218334759
• gnomAD v2: 19-7152877-G-C
• gnomAD v4: 19-7152866-G-C
• MyVariant Identifiers: chr19:g.7152877G>C (hg19) ; chr19:g.7152866G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7152866G>C , CM000681.2:g.7152866G>C	GRCh38
NC_000019.9:g.7152877G>C , CM000681.1:g.7152877G>C	GRCh37
NC_000019.8:g.7103877G>C	NCBI36
NG_008852.2:g.146135C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2091C>G MANE Select	ENSP00000303830.4:p.His697Gln
ENST00000302850.9:c.2091C>G	ENSP00000303830.4:p.His697Gln
ENST00000341500.9:c.2091C>G	ENSP00000342838.4:p.His697Gln
ENST00000598216.1:n.2066C>G
NM_000208.2:c.2091C>G	NP_000199.2:p.His697Gln
NM_000208.3:c.2091C>G	NP_000199.2:p.His697Gln
NM_001079817.1:c.2091C>G	NP_001073285.1:p.His697Gln
NM_001079817.2:c.2091C>G	NP_001073285.1:p.His697Gln
XM_011527988.1:c.2169C>G	XP_011526290.1:p.His723Gln
XM_011527989.1:c.2169C>G	XP_011526291.1:p.His723Gln
XM_011527988.2:c.2091C>G	XP_011526290.2:p.His697Gln
XM_011527989.3:c.2091C>G	XP_011526291.2:p.His697Gln
NM_000208.4:c.2091C>G MANE Select	NP_000199.2:p.His697Gln
NM_001079817.3:c.2091C>G	NP_001073285.1:p.His697Gln