Canonical Allele Identifier: CA505217542

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7132239T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132228T>G , CM000681.2:g.7132228T>G	GRCh38
NC_000019.9:g.7132239T>G , CM000681.1:g.7132239T>G	GRCh37
NC_000019.8:g.7083239T>G	NCBI36
NG_008852.2:g.166773A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2772A>C MANE Select	ENSP00000303830.4:p.Arg924=
ENST00000302850.9:c.2772A>C	ENSP00000303830.4:p.Arg924=
ENST00000341500.9:c.2736A>C	ENSP00000342838.4:p.Arg912=
NM_000208.2:c.2772A>C	NP_000199.2:p.Arg924=
NM_000208.3:c.2772A>C	NP_000199.2:p.Arg924=
NM_001079817.1:c.2736A>C	NP_001073285.1:p.Arg912=
NM_001079817.2:c.2736A>C	NP_001073285.1:p.Arg912=
XM_011527988.1:c.2850A>C	XP_011526290.1:p.Arg950=
XM_011527989.1:c.2814A>C	XP_011526291.1:p.Arg938=
XM_011527988.2:c.2772A>C	XP_011526290.2:p.Arg924=
XM_011527989.3:c.2736A>C	XP_011526291.2:p.Arg912=
NM_000208.4:c.2772A>C MANE Select	NP_000199.2:p.Arg924=
NM_001079817.3:c.2736A>C	NP_001073285.1:p.Arg912=