Canonical Allele Identifier: CA403671485

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125535A>G (hg19) ; chr19:g.7125524A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125524A>G , CM000681.2:g.7125524A>G	GRCh38
NC_000019.9:g.7125535A>G , CM000681.1:g.7125535A>G	GRCh37
NC_000019.8:g.7076535A>G	NCBI36
NG_008852.2:g.173477T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3017T>C MANE Select	ENSP00000303830.4:p.Phe1006Ser
ENST00000302850.9:c.3017T>C	ENSP00000303830.4:p.Phe1006Ser
ENST00000341500.9:c.2981T>C	ENSP00000342838.4:p.Phe994Ser
NM_000208.2:c.3017T>C	NP_000199.2:p.Phe1006Ser
NM_000208.3:c.3017T>C	NP_000199.2:p.Phe1006Ser
NM_001079817.1:c.2981T>C	NP_001073285.1:p.Phe994Ser
NM_001079817.2:c.2981T>C	NP_001073285.1:p.Phe994Ser
XM_011527988.1:c.3092T>C	XP_011526290.1:p.Phe1031Ser
XM_011527989.1:c.3056T>C	XP_011526291.1:p.Phe1019Ser
XM_011527988.2:c.3014T>C	XP_011526290.2:p.Phe1005Ser
XM_011527989.3:c.2978T>C	XP_011526291.2:p.Phe993Ser
NM_000208.4:c.3017T>C MANE Select	NP_000199.2:p.Phe1006Ser
NM_001079817.3:c.2981T>C	NP_001073285.1:p.Phe994Ser