Canonical Allele Identifier: CA2320780918

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7152559_7152560delinsTC , CM000681.2:g.7152559_7152560delinsTC	GRCh38
NC_000019.9:g.7152570_7152571delinsTC , CM000681.1:g.7152570_7152571delinsTC	GRCh37
NC_000019.8:g.7103570_7103571delinsTC	NCBI36
NG_008852.2:g.146441_146442delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2231+166_2231+167delinsGA MANE Select	ENSP00000303830.4:n.2231+166_2231+167delinsGA
ENST00000302850.9:c.2231+166_2231+167delinsGA	ENSP00000303830.4:n.2231+166_2231+167delinsGA
ENST00000341500.9:c.2231+166_2231+167delinsGA	ENSP00000342838.4:n.2231+166_2231+167delinsGA
ENST00000598216.1:n.2372_2373delinsGA
NM_000208.2:c.2231+166_2231+167delinsGA	NP_000199.2:n.2231+166_2231+167delinsGA
NM_000208.3:c.2231+166_2231+167delinsGA	NP_000199.2:n.2231+166_2231+167delinsGA
NM_001079817.1:c.2231+166_2231+167delinsGA	NP_001073285.1:n.2231+166_2231+167delinsGA
NM_001079817.2:c.2231+166_2231+167delinsGA	NP_001073285.1:n.2231+166_2231+167delinsGA
XM_011527988.1:c.2309+166_2309+167delinsGA	XP_011526290.1:n.2309+166_2309+167delinsGA
XM_011527989.1:c.2309+166_2309+167delinsGA	XP_011526291.1:n.2309+166_2309+167delinsGA
XM_011527988.2:c.2231+166_2231+167delinsGA	XP_011526290.2:n.2231+166_2231+167delinsGA
XM_011527989.3:c.2231+166_2231+167delinsGA	XP_011526291.2:n.2231+166_2231+167delinsGA
NM_000208.4:c.2231+166_2231+167delinsGA MANE Select	NP_000199.2:n.2231+166_2231+167delinsGA
NM_001079817.3:c.2231+166_2231+167delinsGA	NP_001073285.1:n.2231+166_2231+167delinsGA