Canonical Allele Identifier: CA2320779414

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7150281_7150283delinsAGT , CM000681.2:g.7150281_7150283delinsAGT	GRCh38
NC_000019.9:g.7150292_7150294delinsAGT , CM000681.1:g.7150292_7150294delinsAGT	GRCh37
NC_000019.8:g.7101292_7101294delinsAGT	NCBI36
NG_008852.2:g.148718_148720delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2267+214_2267+216delinsACT MANE Select	ENSP00000303830.4:n.2267+214_2267+216delinsACT
ENST00000302850.9:c.2267+214_2267+216delinsACT	ENSP00000303830.4:n.2267+214_2267+216delinsACT
ENST00000341500.9:c.2231+2443_2231+2445delinsACT	ENSP00000342838.4:n.2231+2443_2231+2445delinsACT
NM_000208.2:c.2267+214_2267+216delinsACT	NP_000199.2:n.2267+214_2267+216delinsACT
NM_000208.3:c.2267+214_2267+216delinsACT	NP_000199.2:n.2267+214_2267+216delinsACT
NM_001079817.1:c.2231+2443_2231+2445delinsACT	NP_001073285.1:n.2231+2443_2231+2445delinsACT
NM_001079817.2:c.2231+2443_2231+2445delinsACT	NP_001073285.1:n.2231+2443_2231+2445delinsACT
XM_011527988.1:c.2345+214_2345+216delinsACT	XP_011526290.1:n.2345+214_2345+216delinsACT
XM_011527989.1:c.2309+2443_2309+2445delinsACT	XP_011526291.1:n.2309+2443_2309+2445delinsACT
XM_011527988.2:c.2267+214_2267+216delinsACT	XP_011526290.2:n.2267+214_2267+216delinsACT
XM_011527989.3:c.2231+2443_2231+2445delinsACT	XP_011526291.2:n.2231+2443_2231+2445delinsACT
NM_000208.4:c.2267+214_2267+216delinsACT MANE Select	NP_000199.2:n.2267+214_2267+216delinsACT
NM_001079817.3:c.2231+2443_2231+2445delinsACT	NP_001073285.1:n.2231+2443_2231+2445delinsACT