Canonical Allele Identifier: CA2320796186

Gene: INSR

Linked Data

• dbSNP Id: rs1974380891

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184699_7184701del , CM000681.2:g.7184699_7184701del	GRCh38
NC_000019.9:g.7184710_7184712del , CM000681.1:g.7184710_7184712del	GRCh37
NC_000019.8:g.7135710_7135712del	NCBI36
NG_008852.2:g.114302_114304del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-62_653-60del MANE Select	ENSP00000303830.4:n.653-62_653-60del
ENST00000302850.9:c.653-62_653-60del	ENSP00000303830.4:n.653-62_653-60del
ENST00000341500.9:c.653-62_653-60del	ENSP00000342838.4:n.653-62_653-60del
ENST00000598216.1:n.628-62_628-60del
NM_000208.2:c.653-62_653-60del	NP_000199.2:n.653-62_653-60del
NM_000208.3:c.653-62_653-60del	NP_000199.2:n.653-62_653-60del
NM_001079817.1:c.653-62_653-60del	NP_001073285.1:n.653-62_653-60del
NM_001079817.2:c.653-62_653-60del	NP_001073285.1:n.653-62_653-60del
XM_011527988.1:c.731-62_731-60del	XP_011526290.1:n.731-62_731-60del
XM_011527989.1:c.731-62_731-60del	XP_011526291.1:n.731-62_731-60del
XM_011527988.2:c.653-62_653-60del	XP_011526290.2:n.653-62_653-60del
XM_011527989.3:c.653-62_653-60del	XP_011526291.2:n.653-62_653-60del
NM_000208.4:c.653-62_653-60del MANE Select	NP_000199.2:n.653-62_653-60del
NM_001079817.3:c.653-62_653-60del	NP_001073285.1:n.653-62_653-60del