Canonical Allele Identifier: CA403672030

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7132231G>A (hg19) ; chr19:g.7132220G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132220G>A , CM000681.2:g.7132220G>A	GRCh38
NC_000019.9:g.7132231G>A , CM000681.1:g.7132231G>A	GRCh37
NC_000019.8:g.7083231G>A	NCBI36
NG_008852.2:g.166781C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2780C>T MANE Select	ENSP00000303830.4:p.Ala927Val
ENST00000302850.9:c.2780C>T	ENSP00000303830.4:p.Ala927Val
ENST00000341500.9:c.2744C>T	ENSP00000342838.4:p.Ala915Val
NM_000208.2:c.2780C>T	NP_000199.2:p.Ala927Val
NM_000208.3:c.2780C>T	NP_000199.2:p.Ala927Val
NM_001079817.1:c.2744C>T	NP_001073285.1:p.Ala915Val
NM_001079817.2:c.2744C>T	NP_001073285.1:p.Ala915Val
XM_011527988.1:c.2858C>T	XP_011526290.1:p.Ala953Val
XM_011527989.1:c.2822C>T	XP_011526291.1:p.Ala941Val
XM_011527988.2:c.2780C>T	XP_011526290.2:p.Ala927Val
XM_011527989.3:c.2744C>T	XP_011526291.2:p.Ala915Val
NM_000208.4:c.2780C>T MANE Select	NP_000199.2:p.Ala927Val
NM_001079817.3:c.2744C>T	NP_001073285.1:p.Ala915Val