Canonical Allele Identifier: CA2587926428

Gene: INSR

Linked Data

• gnomAD v4: 19-7184683-T-TAAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184686_7184687insGAAA , CM000681.2:g.7184686_7184687insGAAA	GRCh38
NC_000019.9:g.7184697_7184698insGAAA , CM000681.1:g.7184697_7184698insGAAA	GRCh37
NC_000019.8:g.7135697_7135698insGAAA	NCBI36
NG_008852.2:g.114317_114318insCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-47_653-46insCTTT MANE Select	ENSP00000303830.4:n.653-47_653-46insCTTT
ENST00000302850.9:c.653-47_653-46insCTTT	ENSP00000303830.4:n.653-47_653-46insCTTT
ENST00000341500.9:c.653-47_653-46insCTTT	ENSP00000342838.4:n.653-47_653-46insCTTT
ENST00000598216.1:n.628-47_628-46insCTTT
NM_000208.2:c.653-47_653-46insCTTT	NP_000199.2:n.653-47_653-46insCTTT
NM_000208.3:c.653-47_653-46insCTTT	NP_000199.2:n.653-47_653-46insCTTT
NM_001079817.1:c.653-47_653-46insCTTT	NP_001073285.1:n.653-47_653-46insCTTT
NM_001079817.2:c.653-47_653-46insCTTT	NP_001073285.1:n.653-47_653-46insCTTT
XM_011527988.1:c.731-47_731-46insCTTT	XP_011526290.1:n.731-47_731-46insCTTT
XM_011527989.1:c.731-47_731-46insCTTT	XP_011526291.1:n.731-47_731-46insCTTT
XM_011527988.2:c.653-47_653-46insCTTT	XP_011526290.2:n.653-47_653-46insCTTT
XM_011527989.3:c.653-47_653-46insCTTT	XP_011526291.2:n.653-47_653-46insCTTT
NM_000208.4:c.653-47_653-46insCTTT MANE Select	NP_000199.2:n.653-47_653-46insCTTT
NM_001079817.3:c.653-47_653-46insCTTT	NP_001073285.1:n.653-47_653-46insCTTT