Canonical Allele Identifier: CA403671082

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125344C>T (hg19) ; chr19:g.7125333C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125333C>T , CM000681.2:g.7125333C>T	GRCh38
NC_000019.9:g.7125344C>T , CM000681.1:g.7125344C>T	GRCh37
NC_000019.8:g.7076344C>T	NCBI36
NG_008852.2:g.173668G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3208G>A MANE Select	ENSP00000303830.4:p.Glu1070Lys
ENST00000302850.9:c.3208G>A	ENSP00000303830.4:p.Glu1070Lys
ENST00000341500.9:c.3172G>A	ENSP00000342838.4:p.Glu1058Lys
ENST00000593970.1:n.54G>A
NM_000208.2:c.3208G>A	NP_000199.2:p.Glu1070Lys
NM_000208.3:c.3208G>A	NP_000199.2:p.Glu1070Lys
NM_001079817.1:c.3172G>A	NP_001073285.1:p.Glu1058Lys
NM_001079817.2:c.3172G>A	NP_001073285.1:p.Glu1058Lys
XM_011527988.1:c.3283G>A	XP_011526290.1:p.Glu1095Lys
XM_011527989.1:c.3247G>A	XP_011526291.1:p.Glu1083Lys
XM_011527988.2:c.3205G>A	XP_011526290.2:p.Glu1069Lys
XM_011527989.3:c.3169G>A	XP_011526291.2:p.Glu1057Lys
NM_000208.4:c.3208G>A MANE Select	NP_000199.2:p.Glu1070Lys
NM_001079817.3:c.3172G>A	NP_001073285.1:p.Glu1058Lys