Canonical Allele Identifier: CA403671432

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125511T>C (hg19) ; chr19:g.7125500T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125500T>C , CM000681.2:g.7125500T>C	GRCh38
NC_000019.9:g.7125511T>C , CM000681.1:g.7125511T>C	GRCh37
NC_000019.8:g.7076511T>C	NCBI36
NG_008852.2:g.173501A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3041A>G MANE Select	ENSP00000303830.4:p.Asp1014Gly
ENST00000302850.9:c.3041A>G	ENSP00000303830.4:p.Asp1014Gly
ENST00000341500.9:c.3005A>G	ENSP00000342838.4:p.Asp1002Gly
NM_000208.2:c.3041A>G	NP_000199.2:p.Asp1014Gly
NM_000208.3:c.3041A>G	NP_000199.2:p.Asp1014Gly
NM_001079817.1:c.3005A>G	NP_001073285.1:p.Asp1002Gly
NM_001079817.2:c.3005A>G	NP_001073285.1:p.Asp1002Gly
XM_011527988.1:c.3116A>G	XP_011526290.1:p.Asp1039Gly
XM_011527989.1:c.3080A>G	XP_011526291.1:p.Asp1027Gly
XM_011527988.2:c.3038A>G	XP_011526290.2:p.Asp1013Gly
XM_011527989.3:c.3002A>G	XP_011526291.2:p.Asp1001Gly
NM_000208.4:c.3041A>G MANE Select	NP_000199.2:p.Asp1014Gly
NM_001079817.3:c.3005A>G	NP_001073285.1:p.Asp1002Gly