Canonical Allele Identifier: CA403671379

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125487T>C (hg19) ; chr19:g.7125476T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125476T>C , CM000681.2:g.7125476T>C	GRCh38
NC_000019.9:g.7125487T>C , CM000681.1:g.7125487T>C	GRCh37
NC_000019.8:g.7076487T>C	NCBI36
NG_008852.2:g.173525A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3065A>G MANE Select	ENSP00000303830.4:p.Lys1022Arg
ENST00000302850.9:c.3065A>G	ENSP00000303830.4:p.Lys1022Arg
ENST00000341500.9:c.3029A>G	ENSP00000342838.4:p.Lys1010Arg
NM_000208.2:c.3065A>G	NP_000199.2:p.Lys1022Arg
NM_000208.3:c.3065A>G	NP_000199.2:p.Lys1022Arg
NM_001079817.1:c.3029A>G	NP_001073285.1:p.Lys1010Arg
NM_001079817.2:c.3029A>G	NP_001073285.1:p.Lys1010Arg
XM_011527988.1:c.3140A>G	XP_011526290.1:p.Lys1047Arg
XM_011527989.1:c.3104A>G	XP_011526291.1:p.Lys1035Arg
XM_011527988.2:c.3062A>G	XP_011526290.2:p.Lys1021Arg
XM_011527989.3:c.3026A>G	XP_011526291.2:p.Lys1009Arg
NM_000208.4:c.3065A>G MANE Select	NP_000199.2:p.Lys1022Arg
NM_001079817.3:c.3029A>G	NP_001073285.1:p.Lys1010Arg