Canonical Allele Identifier: CA403671254

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125427G>T (hg19) ; chr19:g.7125416G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125416G>T , CM000681.2:g.7125416G>T	GRCh38
NC_000019.9:g.7125427G>T , CM000681.1:g.7125427G>T	GRCh37
NC_000019.8:g.7076427G>T	NCBI36
NG_008852.2:g.173585C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3125C>A MANE Select	ENSP00000303830.4:p.Ala1042Asp
ENST00000302850.9:c.3125C>A	ENSP00000303830.4:p.Ala1042Asp
ENST00000341500.9:c.3089C>A	ENSP00000342838.4:p.Ala1030Asp
NM_000208.2:c.3125C>A	NP_000199.2:p.Ala1042Asp
NM_000208.3:c.3125C>A	NP_000199.2:p.Ala1042Asp
NM_001079817.1:c.3089C>A	NP_001073285.1:p.Ala1030Asp
NM_001079817.2:c.3089C>A	NP_001073285.1:p.Ala1030Asp
XM_011527988.1:c.3200C>A	XP_011526290.1:p.Ala1067Asp
XM_011527989.1:c.3164C>A	XP_011526291.1:p.Ala1055Asp
XM_011527988.2:c.3122C>A	XP_011526290.2:p.Ala1041Asp
XM_011527989.3:c.3086C>A	XP_011526291.2:p.Ala1029Asp
NM_000208.4:c.3125C>A MANE Select	NP_000199.2:p.Ala1042Asp
NM_001079817.3:c.3089C>A	NP_001073285.1:p.Ala1030Asp