Canonical Allele Identifier: CA403669378

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7120661T>G (hg19) ; chr19:g.7120650T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3629A>C MANE Select	ENSP00000303830.4:p.Asp1210Ala
ENST00000302850.9:c.3629A>C	ENSP00000303830.4:p.Asp1210Ala
ENST00000341500.9:c.3593A>C	ENSP00000342838.4:p.Asp1198Ala
ENST00000601099.1:n.540A>C
NM_000208.2:c.3629A>C	NP_000199.2:p.Asp1210Ala
NM_000208.3:c.3629A>C	NP_000199.2:p.Asp1210Ala
NM_001079817.1:c.3593A>C	NP_001073285.1:p.Asp1198Ala
NM_001079817.2:c.3593A>C	NP_001073285.1:p.Asp1198Ala
XM_011527988.1:c.3704A>C	XP_011526290.1:p.Asp1235Ala
XM_011527989.1:c.3668A>C	XP_011526291.1:p.Asp1223Ala
XM_011527988.2:c.3626A>C	XP_011526290.2:p.Asp1209Ala
XM_011527989.3:c.3590A>C	XP_011526291.2:p.Asp1197Ala
NM_000208.4:c.3629A>C MANE Select	NP_000199.2:p.Asp1210Ala
NM_001079817.3:c.3593A>C	NP_001073285.1:p.Asp1198Ala