Canonical Allele Identifier: CA403671250

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125425T>A (hg19) ; chr19:g.7125414T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125414T>A , CM000681.2:g.7125414T>A	GRCh38
NC_000019.9:g.7125425T>A , CM000681.1:g.7125425T>A	GRCh37
NC_000019.8:g.7076425T>A	NCBI36
NG_008852.2:g.173587A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3127A>T MANE Select	ENSP00000303830.4:p.Arg1043Trp
ENST00000302850.9:c.3127A>T	ENSP00000303830.4:p.Arg1043Trp
ENST00000341500.9:c.3091A>T	ENSP00000342838.4:p.Arg1031Trp
NM_000208.2:c.3127A>T	NP_000199.2:p.Arg1043Trp
NM_000208.3:c.3127A>T	NP_000199.2:p.Arg1043Trp
NM_001079817.1:c.3091A>T	NP_001073285.1:p.Arg1031Trp
NM_001079817.2:c.3091A>T	NP_001073285.1:p.Arg1031Trp
XM_011527988.1:c.3202A>T	XP_011526290.1:p.Arg1068Trp
XM_011527989.1:c.3166A>T	XP_011526291.1:p.Arg1056Trp
XM_011527988.2:c.3124A>T	XP_011526290.2:p.Arg1042Trp
XM_011527989.3:c.3088A>T	XP_011526291.2:p.Arg1030Trp
NM_000208.4:c.3127A>T MANE Select	NP_000199.2:p.Arg1043Trp
NM_001079817.3:c.3091A>T	NP_001073285.1:p.Arg1031Trp