Canonical Allele Identifier: CA403666402

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7166268C>T (hg19) ; chr19:g.7166257C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166257C>T , CM000681.2:g.7166257C>T	GRCh38
NC_000019.9:g.7166268C>T , CM000681.1:g.7166268C>T	GRCh37
NC_000019.8:g.7117268C>T	NCBI36
NG_008852.2:g.132744G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1758G>A MANE Select	ENSP00000303830.4:p.Trp586Ter
ENST00000302850.9:c.1758G>A	ENSP00000303830.4:p.Trp586Ter
ENST00000341500.9:c.1758G>A	ENSP00000342838.4:p.Trp586Ter
ENST00000598216.1:n.1733G>A
ENST00000600492.1:c.159G>A	ENSP00000473170.1:p.Trp53Ter
NM_000208.2:c.1758G>A	NP_000199.2:p.Trp586Ter
NM_000208.3:c.1758G>A	NP_000199.2:p.Trp586Ter
NM_001079817.1:c.1758G>A	NP_001073285.1:p.Trp586Ter
NM_001079817.2:c.1758G>A	NP_001073285.1:p.Trp586Ter
XM_011527988.1:c.1836G>A	XP_011526290.1:p.Trp612Ter
XM_011527989.1:c.1836G>A	XP_011526291.1:p.Trp612Ter
XM_011527988.2:c.1758G>A	XP_011526290.2:p.Trp586Ter
XM_011527989.3:c.1758G>A	XP_011526291.2:p.Trp586Ter
NM_000208.4:c.1758G>A MANE Select	NP_000199.2:p.Trp586Ter
NM_001079817.3:c.1758G>A	NP_001073285.1:p.Trp586Ter