Canonical Allele Identifier: CA993124955

Gene: INSR

Linked Data

• dbSNP Id: rs1974380046
• gnomAD v3: 19-7184675-TAAA-T
• gnomAD v4: 19-7184675-TAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184676_7184678del , CM000681.2:g.7184676_7184678del	GRCh38
NC_000019.9:g.7184687_7184689del , CM000681.1:g.7184687_7184689del	GRCh37
NC_000019.8:g.7135687_7135689del	NCBI36
NG_008852.2:g.114323_114325del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-41_653-39del MANE Select	ENSP00000303830.4:n.653-41_653-39del
ENST00000302850.9:c.653-41_653-39del	ENSP00000303830.4:n.653-41_653-39del
ENST00000341500.9:c.653-41_653-39del	ENSP00000342838.4:n.653-41_653-39del
ENST00000598216.1:n.628-41_628-39del
NM_000208.2:c.653-41_653-39del	NP_000199.2:n.653-41_653-39del
NM_000208.3:c.653-41_653-39del	NP_000199.2:n.653-41_653-39del
NM_001079817.1:c.653-41_653-39del	NP_001073285.1:n.653-41_653-39del
NM_001079817.2:c.653-41_653-39del	NP_001073285.1:n.653-41_653-39del
XM_011527988.1:c.731-41_731-39del	XP_011526290.1:n.731-41_731-39del
XM_011527989.1:c.731-41_731-39del	XP_011526291.1:n.731-41_731-39del
XM_011527988.2:c.653-41_653-39del	XP_011526290.2:n.653-41_653-39del
XM_011527989.3:c.653-41_653-39del	XP_011526291.2:n.653-41_653-39del
NM_000208.4:c.653-41_653-39del MANE Select	NP_000199.2:n.653-41_653-39del
NM_001079817.3:c.653-41_653-39del	NP_001073285.1:n.653-41_653-39del