Canonical Allele Identifier: CA2587922191

Gene: INSR

Linked Data

• gnomAD v4: 19-7125677-CCGAGAACAGGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125679_7125689del , CM000681.2:g.7125679_7125689del	GRCh38
NC_000019.9:g.7125690_7125700del , CM000681.1:g.7125690_7125700del	GRCh37
NC_000019.8:g.7076690_7076700del	NCBI36
NG_008852.2:g.173313_173323del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3014-161_3014-151del MANE Select	ENSP00000303830.4:n.3014-161_3014-151del
ENST00000302850.9:c.3014-161_3014-151del	ENSP00000303830.4:n.3014-161_3014-151del
ENST00000341500.9:c.2978-161_2978-151del	ENSP00000342838.4:n.2978-161_2978-151del
NM_000208.2:c.3014-161_3014-151del	NP_000199.2:n.3014-161_3014-151del
NM_000208.3:c.3014-161_3014-151del	NP_000199.2:n.3014-161_3014-151del
NM_001079817.1:c.2978-161_2978-151del	NP_001073285.1:n.2978-161_2978-151del
NM_001079817.2:c.2978-161_2978-151del	NP_001073285.1:n.2978-161_2978-151del
XM_011527988.1:c.3089-161_3089-151del	XP_011526290.1:n.3089-161_3089-151del
XM_011527989.1:c.3053-161_3053-151del	XP_011526291.1:n.3053-161_3053-151del
XM_011527988.2:c.3011-161_3011-151del	XP_011526290.2:n.3011-161_3011-151del
XM_011527989.3:c.2975-161_2975-151del	XP_011526291.2:n.2975-161_2975-151del
NM_000208.4:c.3014-161_3014-151del MANE Select	NP_000199.2:n.3014-161_3014-151del
NM_001079817.3:c.2978-161_2978-151del	NP_001073285.1:n.2978-161_2978-151del