Canonical Allele Identifier: CA403671771

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128914A>G (hg19) ; chr19:g.7128903A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128903A>G , CM000681.2:g.7128903A>G	GRCh38
NC_000019.9:g.7128914A>G , CM000681.1:g.7128914A>G	GRCh37
NC_000019.8:g.7079914A>G	NCBI36
NG_008852.2:g.170098T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2894T>C MANE Select	ENSP00000303830.4:p.Val965Ala
ENST00000302850.9:c.2894T>C	ENSP00000303830.4:p.Val965Ala
ENST00000341500.9:c.2858T>C	ENSP00000342838.4:p.Val953Ala
NM_000208.2:c.2894T>C	NP_000199.2:p.Val965Ala
NM_000208.3:c.2894T>C	NP_000199.2:p.Val965Ala
NM_001079817.1:c.2858T>C	NP_001073285.1:p.Val953Ala
NM_001079817.2:c.2858T>C	NP_001073285.1:p.Val953Ala
XM_011527988.1:c.2969T>C	XP_011526290.1:p.Val990Ala
XM_011527989.1:c.2933T>C	XP_011526291.1:p.Val978Ala
XM_011527988.2:c.2891T>C	XP_011526290.2:p.Val964Ala
XM_011527989.3:c.2855T>C	XP_011526291.2:p.Val952Ala
NM_000208.4:c.2894T>C MANE Select	NP_000199.2:p.Val965Ala
NM_001079817.3:c.2858T>C	NP_001073285.1:p.Val953Ala