Canonical Allele Identifier: CA403671764

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128910A>T (hg19) ; chr19:g.7128899A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128899A>T , CM000681.2:g.7128899A>T	GRCh38
NC_000019.9:g.7128910A>T , CM000681.1:g.7128910A>T	GRCh37
NC_000019.8:g.7079910A>T	NCBI36
NG_008852.2:g.170102T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2898T>A MANE Select	ENSP00000303830.4:p.Phe966Leu
ENST00000302850.9:c.2898T>A	ENSP00000303830.4:p.Phe966Leu
ENST00000341500.9:c.2862T>A	ENSP00000342838.4:p.Phe954Leu
NM_000208.2:c.2898T>A	NP_000199.2:p.Phe966Leu
NM_000208.3:c.2898T>A	NP_000199.2:p.Phe966Leu
NM_001079817.1:c.2862T>A	NP_001073285.1:p.Phe954Leu
NM_001079817.2:c.2862T>A	NP_001073285.1:p.Phe954Leu
XM_011527988.1:c.2973T>A	XP_011526290.1:p.Phe991Leu
XM_011527989.1:c.2937T>A	XP_011526291.1:p.Phe979Leu
XM_011527988.2:c.2895T>A	XP_011526290.2:p.Phe965Leu
XM_011527989.3:c.2859T>A	XP_011526291.2:p.Phe953Leu
NM_000208.4:c.2898T>A MANE Select	NP_000199.2:p.Phe966Leu
NM_001079817.3:c.2862T>A	NP_001073285.1:p.Phe954Leu