Canonical Allele Identifier: CA403671453

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125521A>C (hg19) ; chr19:g.7125510A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125510A>C , CM000681.2:g.7125510A>C	GRCh38
NC_000019.9:g.7125521A>C , CM000681.1:g.7125521A>C	GRCh37
NC_000019.8:g.7076521A>C	NCBI36
NG_008852.2:g.173491T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3031T>G MANE Select	ENSP00000303830.4:p.Tyr1011Asp
ENST00000302850.9:c.3031T>G	ENSP00000303830.4:p.Tyr1011Asp
ENST00000341500.9:c.2995T>G	ENSP00000342838.4:p.Tyr999Asp
NM_000208.2:c.3031T>G	NP_000199.2:p.Tyr1011Asp
NM_000208.3:c.3031T>G	NP_000199.2:p.Tyr1011Asp
NM_001079817.1:c.2995T>G	NP_001073285.1:p.Tyr999Asp
NM_001079817.2:c.2995T>G	NP_001073285.1:p.Tyr999Asp
XM_011527988.1:c.3106T>G	XP_011526290.1:p.Tyr1036Asp
XM_011527989.1:c.3070T>G	XP_011526291.1:p.Tyr1024Asp
XM_011527988.2:c.3028T>G	XP_011526290.2:p.Tyr1010Asp
XM_011527989.3:c.2992T>G	XP_011526291.2:p.Tyr998Asp
NM_000208.4:c.3031T>G MANE Select	NP_000199.2:p.Tyr1011Asp
NM_001079817.3:c.2995T>G	NP_001073285.1:p.Tyr999Asp