Canonical Allele Identifier: CA505400211

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125378C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125367C>A , CM000681.2:g.7125367C>A	GRCh38
NC_000019.9:g.7125378C>A , CM000681.1:g.7125378C>A	GRCh37
NC_000019.8:g.7076378C>A	NCBI36
NG_008852.2:g.173634G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3174G>T MANE Select	ENSP00000303830.4:p.Thr1058=
ENST00000302850.9:c.3174G>T	ENSP00000303830.4:p.Thr1058=
ENST00000341500.9:c.3138G>T	ENSP00000342838.4:p.Thr1046=
ENST00000593970.1:n.20G>T
NM_000208.2:c.3174G>T	NP_000199.2:p.Thr1058=
NM_000208.3:c.3174G>T	NP_000199.2:p.Thr1058=
NM_001079817.1:c.3138G>T	NP_001073285.1:p.Thr1046=
NM_001079817.2:c.3138G>T	NP_001073285.1:p.Thr1046=
XM_011527988.1:c.3249G>T	XP_011526290.1:p.Thr1083=
XM_011527989.1:c.3213G>T	XP_011526291.1:p.Thr1071=
XM_011527988.2:c.3171G>T	XP_011526290.2:p.Thr1057=
XM_011527989.3:c.3135G>T	XP_011526291.2:p.Thr1045=
NM_000208.4:c.3174G>T MANE Select	NP_000199.2:p.Thr1058=
NM_001079817.3:c.3138G>T	NP_001073285.1:p.Thr1046=