Canonical Allele Identifier: CA2320779400

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7150256_7150257delinsTC , CM000681.2:g.7150256_7150257delinsTC	GRCh38
NC_000019.9:g.7150267_7150268delinsTC , CM000681.1:g.7150267_7150268delinsTC	GRCh37
NC_000019.8:g.7101267_7101268delinsTC	NCBI36
NG_008852.2:g.148744_148745delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2267+240_2267+241delinsGA MANE Select	ENSP00000303830.4:n.2267+240_2267+241delinsGA
ENST00000302850.9:c.2267+240_2267+241delinsGA	ENSP00000303830.4:n.2267+240_2267+241delinsGA
ENST00000341500.9:c.2231+2469_2231+2470delinsGA	ENSP00000342838.4:n.2231+2469_2231+2470delinsGA
NM_000208.2:c.2267+240_2267+241delinsGA	NP_000199.2:n.2267+240_2267+241delinsGA
NM_000208.3:c.2267+240_2267+241delinsGA	NP_000199.2:n.2267+240_2267+241delinsGA
NM_001079817.1:c.2231+2469_2231+2470delinsGA	NP_001073285.1:n.2231+2469_2231+2470delinsGA
NM_001079817.2:c.2231+2469_2231+2470delinsGA	NP_001073285.1:n.2231+2469_2231+2470delinsGA
XM_011527988.1:c.2345+240_2345+241delinsGA	XP_011526290.1:n.2345+240_2345+241delinsGA
XM_011527989.1:c.2309+2469_2309+2470delinsGA	XP_011526291.1:n.2309+2469_2309+2470delinsGA
XM_011527988.2:c.2267+240_2267+241delinsGA	XP_011526290.2:n.2267+240_2267+241delinsGA
XM_011527989.3:c.2231+2469_2231+2470delinsGA	XP_011526291.2:n.2231+2469_2231+2470delinsGA
NM_000208.4:c.2267+240_2267+241delinsGA MANE Select	NP_000199.2:n.2267+240_2267+241delinsGA
NM_001079817.3:c.2231+2469_2231+2470delinsGA	NP_001073285.1:n.2231+2469_2231+2470delinsGA