Canonical Allele Identifier: CA2320769423

Gene: INSR

Linked Data

• dbSNP Id: rs1599877761

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128788C>G , CM000681.2:g.7128788C>G	GRCh38
NC_000019.9:g.7128799C>G , CM000681.1:g.7128799C>G	GRCh37
NC_000019.8:g.7079799C>G	NCBI36
NG_008852.2:g.170213G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2945+64G>C MANE Select	ENSP00000303830.4:n.2945+64G>C
ENST00000302850.9:c.2945+64G>C	ENSP00000303830.4:n.2945+64G>C
ENST00000341500.9:c.2909+64G>C	ENSP00000342838.4:n.2909+64G>C
NM_000208.2:c.2945+64G>C	NP_000199.2:n.2945+64G>C
NM_000208.3:c.2945+64G>C	NP_000199.2:n.2945+64G>C
NM_001079817.1:c.2909+64G>C	NP_001073285.1:n.2909+64G>C
NM_001079817.2:c.2909+64G>C	NP_001073285.1:n.2909+64G>C
XM_011527988.1:c.3020+64G>C	XP_011526290.1:n.3020+64G>C
XM_011527989.1:c.2984+64G>C	XP_011526291.1:n.2984+64G>C
XM_011527988.2:c.2942+64G>C	XP_011526290.2:n.2942+64G>C
XM_011527989.3:c.2906+64G>C	XP_011526291.2:n.2906+64G>C
NM_000208.4:c.2945+64G>C MANE Select	NP_000199.2:n.2945+64G>C
NM_001079817.3:c.2909+64G>C	NP_001073285.1:n.2909+64G>C