Canonical Allele Identifier: CA2576594992

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7123027del , CM000681.2:g.7123027del	GRCh38
NC_000019.9:g.7123038del , CM000681.1:g.7123038del	GRCh37
NC_000019.8:g.7074038del	NCBI36
NG_008852.2:g.175975del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3259-37del MANE Select	ENSP00000303830.4:n.3259-37del
ENST00000302850.9:c.3259-37del	ENSP00000303830.4:n.3259-37del
ENST00000341500.9:c.3223-37del	ENSP00000342838.4:n.3223-37del
ENST00000593970.1:n.105-37del
ENST00000601099.1:n.133del
NM_000208.2:c.3259-37del	NP_000199.2:n.3259-37del
NM_000208.3:c.3259-37del	NP_000199.2:n.3259-37del
NM_001079817.1:c.3223-37del	NP_001073285.1:n.3223-37del
NM_001079817.2:c.3223-37del	NP_001073285.1:n.3223-37del
XM_011527988.1:c.3334-37del	XP_011526290.1:n.3334-37del
XM_011527989.1:c.3298-37del	XP_011526291.1:n.3298-37del
XM_011527988.2:c.3256-37del	XP_011526290.2:n.3256-37del
XM_011527989.3:c.3220-37del	XP_011526291.2:n.3220-37del
NM_000208.4:c.3259-37del MANE Select	NP_000199.2:n.3259-37del
NM_001079817.3:c.3223-37del	NP_001073285.1:n.3223-37del