Canonical Allele Identifier: CA505400212

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125381C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125370C>T , CM000681.2:g.7125370C>T	GRCh38
NC_000019.9:g.7125381C>T , CM000681.1:g.7125381C>T	GRCh37
NC_000019.8:g.7076381C>T	NCBI36
NG_008852.2:g.173631G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3171G>A MANE Select	ENSP00000303830.4:p.Lys1057=
ENST00000302850.9:c.3171G>A	ENSP00000303830.4:p.Lys1057=
ENST00000341500.9:c.3135G>A	ENSP00000342838.4:p.Lys1045=
ENST00000593970.1:n.17G>A
NM_000208.2:c.3171G>A	NP_000199.2:p.Lys1057=
NM_000208.3:c.3171G>A	NP_000199.2:p.Lys1057=
NM_001079817.1:c.3135G>A	NP_001073285.1:p.Lys1045=
NM_001079817.2:c.3135G>A	NP_001073285.1:p.Lys1045=
XM_011527988.1:c.3246G>A	XP_011526290.1:p.Lys1082=
XM_011527989.1:c.3210G>A	XP_011526291.1:p.Lys1070=
XM_011527988.2:c.3168G>A	XP_011526290.2:p.Lys1056=
XM_011527989.3:c.3132G>A	XP_011526291.2:p.Lys1044=
NM_000208.4:c.3171G>A MANE Select	NP_000199.2:p.Lys1057=
NM_001079817.3:c.3135G>A	NP_001073285.1:p.Lys1045=