Canonical Allele Identifier: CA403669379

Gene: INSR

Linked Data

• dbSNP Id: rs1251723810
• gnomAD v2: 19-7120661-T-C
• MyVariant Identifiers: chr19:g.7120661T>C (hg19) ; chr19:g.7120650T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120650T>C , CM000681.2:g.7120650T>C	GRCh38
NC_000019.9:g.7120661T>C , CM000681.1:g.7120661T>C	GRCh37
NC_000019.8:g.7071661T>C	NCBI36
NG_008852.2:g.178351A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3629A>G MANE Select	ENSP00000303830.4:p.Asp1210Gly
ENST00000302850.9:c.3629A>G	ENSP00000303830.4:p.Asp1210Gly
ENST00000341500.9:c.3593A>G	ENSP00000342838.4:p.Asp1198Gly
ENST00000601099.1:n.540A>G
NM_000208.2:c.3629A>G	NP_000199.2:p.Asp1210Gly
NM_000208.3:c.3629A>G	NP_000199.2:p.Asp1210Gly
NM_001079817.1:c.3593A>G	NP_001073285.1:p.Asp1198Gly
NM_001079817.2:c.3593A>G	NP_001073285.1:p.Asp1198Gly
XM_011527988.1:c.3704A>G	XP_011526290.1:p.Asp1235Gly
XM_011527989.1:c.3668A>G	XP_011526291.1:p.Asp1223Gly
XM_011527988.2:c.3626A>G	XP_011526290.2:p.Asp1209Gly
XM_011527989.3:c.3590A>G	XP_011526291.2:p.Asp1197Gly
NM_000208.4:c.3629A>G MANE Select	NP_000199.2:p.Asp1210Gly
NM_001079817.3:c.3593A>G	NP_001073285.1:p.Asp1198Gly