Canonical Allele Identifier: CA2576595384

Gene: INSR

Linked Data

• gnomAD v4: 19-7184226-TGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184227_7184228del , CM000681.2:g.7184227_7184228del	GRCh38
NC_000019.9:g.7184238_7184239del , CM000681.1:g.7184238_7184239del	GRCh37
NC_000019.8:g.7135238_7135239del	NCBI36
NG_008852.2:g.114773_114774del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.974+88_974+89del MANE Select	ENSP00000303830.4:n.974+88_974+89del
ENST00000302850.9:c.974+88_974+89del	ENSP00000303830.4:n.974+88_974+89del
ENST00000341500.9:c.974+88_974+89del	ENSP00000342838.4:n.974+88_974+89del
ENST00000598216.1:n.949+88_949+89del
NM_000208.2:c.974+88_974+89del	NP_000199.2:n.974+88_974+89del
NM_000208.3:c.974+88_974+89del	NP_000199.2:n.974+88_974+89del
NM_001079817.1:c.974+88_974+89del	NP_001073285.1:n.974+88_974+89del
NM_001079817.2:c.974+88_974+89del	NP_001073285.1:n.974+88_974+89del
XM_011527988.1:c.1052+88_1052+89del	XP_011526290.1:n.1052+88_1052+89del
XM_011527989.1:c.1052+88_1052+89del	XP_011526291.1:n.1052+88_1052+89del
XM_011527988.2:c.974+88_974+89del	XP_011526290.2:n.974+88_974+89del
XM_011527989.3:c.974+88_974+89del	XP_011526291.2:n.974+88_974+89del
NM_000208.4:c.974+88_974+89del MANE Select	NP_000199.2:n.974+88_974+89del
NM_001079817.3:c.974+88_974+89del	NP_001073285.1:n.974+88_974+89del