Canonical Allele Identifier: CA2735472039

Gene: INSR

Linked Data

• dbSNP Id: rs2144890686

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7152696del , CM000681.2:g.7152696del	GRCh38
NC_000019.9:g.7152707del , CM000681.1:g.7152707del	GRCh37
NC_000019.8:g.7103707del	NCBI36
NG_008852.2:g.146307del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2231+32del MANE Select	ENSP00000303830.4:n.2231+32del
ENST00000302850.9:c.2231+32del	ENSP00000303830.4:n.2231+32del
ENST00000341500.9:c.2231+32del	ENSP00000342838.4:n.2231+32del
ENST00000598216.1:n.2238del
NM_000208.2:c.2231+32del	NP_000199.2:n.2231+32del
NM_000208.3:c.2231+32del	NP_000199.2:n.2231+32del
NM_001079817.1:c.2231+32del	NP_001073285.1:n.2231+32del
NM_001079817.2:c.2231+32del	NP_001073285.1:n.2231+32del
XM_011527988.1:c.2309+32del	XP_011526290.1:n.2309+32del
XM_011527989.1:c.2309+32del	XP_011526291.1:n.2309+32del
XM_011527988.2:c.2231+32del	XP_011526290.2:n.2231+32del
XM_011527989.3:c.2231+32del	XP_011526291.2:n.2231+32del
NM_000208.4:c.2231+32del MANE Select	NP_000199.2:n.2231+32del
NM_001079817.3:c.2231+32del	NP_001073285.1:n.2231+32del