Canonical Allele Identifier: CA2320779441

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7150369_7150374delinsGCTCTC , CM000681.2:g.7150369_7150374delinsGCTCTC	GRCh38
NC_000019.9:g.7150380_7150385delinsGCTCTC , CM000681.1:g.7150380_7150385delinsGCTCTC	GRCh37
NC_000019.8:g.7101380_7101385delinsGCTCTC	NCBI36
NG_008852.2:g.148627_148632delinsGAGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2267+123_2267+128delinsGAGAGC MANE Select	ENSP00000303830.4:n.2267+123_2267+128delinsGAGAGC
ENST00000302850.9:c.2267+123_2267+128delinsGAGAGC	ENSP00000303830.4:n.2267+123_2267+128delinsGAGAGC
ENST00000341500.9:c.2231+2352_2231+2357delinsGAGAGC	ENSP00000342838.4:n.2231+2352_2231+2357delinsGAGAGC
NM_000208.2:c.2267+123_2267+128delinsGAGAGC	NP_000199.2:n.2267+123_2267+128delinsGAGAGC
NM_000208.3:c.2267+123_2267+128delinsGAGAGC	NP_000199.2:n.2267+123_2267+128delinsGAGAGC
NM_001079817.1:c.2231+2352_2231+2357delinsGAGAGC	NP_001073285.1:n.2231+2352_2231+2357delinsGAGAGC
NM_001079817.2:c.2231+2352_2231+2357delinsGAGAGC	NP_001073285.1:n.2231+2352_2231+2357delinsGAGAGC
XM_011527988.1:c.2345+123_2345+128delinsGAGAGC	XP_011526290.1:n.2345+123_2345+128delinsGAGAGC
XM_011527989.1:c.2309+2352_2309+2357delinsGAGAGC	XP_011526291.1:n.2309+2352_2309+2357delinsGAGAGC
XM_011527988.2:c.2267+123_2267+128delinsGAGAGC	XP_011526290.2:n.2267+123_2267+128delinsGAGAGC
XM_011527989.3:c.2231+2352_2231+2357delinsGAGAGC	XP_011526291.2:n.2231+2352_2231+2357delinsGAGAGC
NM_000208.4:c.2267+123_2267+128delinsGAGAGC MANE Select	NP_000199.2:n.2267+123_2267+128delinsGAGAGC
NM_001079817.3:c.2231+2352_2231+2357delinsGAGAGC	NP_001073285.1:n.2231+2352_2231+2357delinsGAGAGC