Canonical Allele Identifier: CA2320769413

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128767_7128768delinsTA , CM000681.2:g.7128767_7128768delinsTA	GRCh38
NC_000019.9:g.7128778_7128779delinsTA , CM000681.1:g.7128778_7128779delinsTA	GRCh37
NC_000019.8:g.7079778_7079779delinsTA	NCBI36
NG_008852.2:g.170233_170234delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2945+84_2945+85delinsTA MANE Select	ENSP00000303830.4:n.2945+84_2945+85delinsTA
ENST00000302850.9:c.2945+84_2945+85delinsTA	ENSP00000303830.4:n.2945+84_2945+85delinsTA
ENST00000341500.9:c.2909+84_2909+85delinsTA	ENSP00000342838.4:n.2909+84_2909+85delinsTA
NM_000208.2:c.2945+84_2945+85delinsTA	NP_000199.2:n.2945+84_2945+85delinsTA
NM_000208.3:c.2945+84_2945+85delinsTA	NP_000199.2:n.2945+84_2945+85delinsTA
NM_001079817.1:c.2909+84_2909+85delinsTA	NP_001073285.1:n.2909+84_2909+85delinsTA
NM_001079817.2:c.2909+84_2909+85delinsTA	NP_001073285.1:n.2909+84_2909+85delinsTA
XM_011527988.1:c.3020+84_3020+85delinsTA	XP_011526290.1:n.3020+84_3020+85delinsTA
XM_011527989.1:c.2984+84_2984+85delinsTA	XP_011526291.1:n.2984+84_2984+85delinsTA
XM_011527988.2:c.2942+84_2942+85delinsTA	XP_011526290.2:n.2942+84_2942+85delinsTA
XM_011527989.3:c.2906+84_2906+85delinsTA	XP_011526291.2:n.2906+84_2906+85delinsTA
NM_000208.4:c.2945+84_2945+85delinsTA MANE Select	NP_000199.2:n.2945+84_2945+85delinsTA
NM_001079817.3:c.2909+84_2909+85delinsTA	NP_001073285.1:n.2909+84_2909+85delinsTA