Canonical Allele Identifier: CA2320779465

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7150412_7150413delinsAC , CM000681.2:g.7150412_7150413delinsAC	GRCh38
NC_000019.9:g.7150423_7150424delinsAC , CM000681.1:g.7150423_7150424delinsAC	GRCh37
NC_000019.8:g.7101423_7101424delinsAC	NCBI36
NG_008852.2:g.148588_148589delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2267+84_2267+85delinsGT MANE Select	ENSP00000303830.4:n.2267+84_2267+85delins...
ENST00000302850.9:c.2267+84_2267+85delinsGT	ENSP00000303830.4:n.2267+84_2267+85delins...
ENST00000341500.9:c.2231+2313_2231+2314delinsGT	ENSP00000342838.4:n.2231+2313_2231+2314de...
NM_000208.2:c.2267+84_2267+85delinsGT	NP_000199.2:n.2267+84_2267+85delinsGT
NM_000208.3:c.2267+84_2267+85delinsGT	NP_000199.2:n.2267+84_2267+85delinsGT
NM_001079817.1:c.2231+2313_2231+2314delinsGT	NP_001073285.1:n.2231+2313_2231+2314delin...
NM_001079817.2:c.2231+2313_2231+2314delinsGT	NP_001073285.1:n.2231+2313_2231+2314delin...
XM_011527988.1:c.2345+84_2345+85delinsGT	XP_011526290.1:n.2345+84_2345+85delinsGT
XM_011527989.1:c.2309+2313_2309+2314delinsGT	XP_011526291.1:n.2309+2313_2309+2314delin...
XM_011527988.2:c.2267+84_2267+85delinsGT	XP_011526290.2:n.2267+84_2267+85delinsGT
XM_011527989.3:c.2231+2313_2231+2314delinsGT	XP_011526291.2:n.2231+2313_2231+2314delin...
NM_000208.4:c.2267+84_2267+85delinsGT MANE Select	NP_000199.2:n.2267+84_2267+85delinsGT
NM_001079817.3:c.2231+2313_2231+2314delinsGT	NP_001073285.1:n.2231+2313_2231+2314delin...