Canonical Allele Identifier: CA403671785

Gene: INSR

Linked Data

• dbSNP Id: rs1972710885
• gnomAD v3: 19-7128909-A-C
• gnomAD v4: 19-7128909-A-C
• MyVariant Identifiers: chr19:g.7128920A>C (hg19) ; chr19:g.7128909A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128909A>C , CM000681.2:g.7128909A>C	GRCh38
NC_000019.9:g.7128920A>C , CM000681.1:g.7128920A>C	GRCh37
NC_000019.8:g.7079920A>C	NCBI36
NG_008852.2:g.170092T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2888T>G MANE Select	ENSP00000303830.4:p.Ile963Ser
ENST00000302850.9:c.2888T>G	ENSP00000303830.4:p.Ile963Ser
ENST00000341500.9:c.2852T>G	ENSP00000342838.4:p.Ile951Ser
NM_000208.2:c.2888T>G	NP_000199.2:p.Ile963Ser
NM_000208.3:c.2888T>G	NP_000199.2:p.Ile963Ser
NM_001079817.1:c.2852T>G	NP_001073285.1:p.Ile951Ser
NM_001079817.2:c.2852T>G	NP_001073285.1:p.Ile951Ser
XM_011527988.1:c.2963T>G	XP_011526290.1:p.Ile988Ser
XM_011527989.1:c.2927T>G	XP_011526291.1:p.Ile976Ser
XM_011527988.2:c.2885T>G	XP_011526290.2:p.Ile962Ser
XM_011527989.3:c.2849T>G	XP_011526291.2:p.Ile950Ser
NM_000208.4:c.2888T>G MANE Select	NP_000199.2:p.Ile963Ser
NM_001079817.3:c.2852T>G	NP_001073285.1:p.Ile951Ser