Canonical Allele Identifier: CA2587921427

Gene: INSR

Linked Data

• gnomAD v4: 19-7120592-TCCATCCAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120601_7120608del , CM000681.2:g.7120601_7120608del	GRCh38
NC_000019.9:g.7120612_7120619del , CM000681.1:g.7120612_7120619del	GRCh37
NC_000019.8:g.7071612_7071619del	NCBI36
NG_008852.2:g.178401_178408del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3659+20_3659+27del MANE Select	ENSP00000303830.4:n.3659+20_3659+27del
ENST00000302850.9:c.3659+20_3659+27del	ENSP00000303830.4:n.3659+20_3659+27del
ENST00000341500.9:c.3623+20_3623+27del	ENSP00000342838.4:n.3623+20_3623+27del
NM_000208.2:c.3659+20_3659+27del	NP_000199.2:n.3659+20_3659+27del
NM_000208.3:c.3659+20_3659+27del	NP_000199.2:n.3659+20_3659+27del
NM_001079817.1:c.3623+20_3623+27del	NP_001073285.1:n.3623+20_3623+27del
NM_001079817.2:c.3623+20_3623+27del	NP_001073285.1:n.3623+20_3623+27del
XM_011527988.1:c.3734+20_3734+27del	XP_011526290.1:n.3734+20_3734+27del
XM_011527989.1:c.3698+20_3698+27del	XP_011526291.1:n.3698+20_3698+27del
XM_011527988.2:c.3656+20_3656+27del	XP_011526290.2:n.3656+20_3656+27del
XM_011527989.3:c.3620+20_3620+27del	XP_011526291.2:n.3620+20_3620+27del
NM_000208.4:c.3659+20_3659+27del MANE Select	NP_000199.2:n.3659+20_3659+27del
NM_001079817.3:c.3623+20_3623+27del	NP_001073285.1:n.3623+20_3623+27del