Canonical Allele Identifier: CA2587925377

Gene: INSR

Linked Data

• gnomAD v4: 19-7167868-TAGAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7167871_7167874del , CM000681.2:g.7167871_7167874del	GRCh38
NC_000019.9:g.7167882_7167885del , CM000681.1:g.7167882_7167885del	GRCh37
NC_000019.8:g.7118882_7118885del	NCBI36
NG_008852.2:g.131129_131132del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.1610+96_1610+99del MANE Select	ENSP00000303830.4:n.1610+96_1610+99del
ENST00000302850.9:c.1610+96_1610+99del	ENSP00000303830.4:n.1610+96_1610+99del
ENST00000341500.9:c.1610+96_1610+99del	ENSP00000342838.4:n.1610+96_1610+99del
ENST00000598216.1:n.1585+96_1585+99del
ENST00000600492.1:c.11+96_11+99del	ENSP00000473170.1:n.11+96_11+99del
NM_000208.2:c.1610+96_1610+99del	NP_000199.2:n.1610+96_1610+99del
NM_000208.3:c.1610+96_1610+99del	NP_000199.2:n.1610+96_1610+99del
NM_001079817.1:c.1610+96_1610+99del	NP_001073285.1:n.1610+96_1610+99del
NM_001079817.2:c.1610+96_1610+99del	NP_001073285.1:n.1610+96_1610+99del
XM_011527988.1:c.1688+96_1688+99del	XP_011526290.1:n.1688+96_1688+99del
XM_011527989.1:c.1688+96_1688+99del	XP_011526291.1:n.1688+96_1688+99del
XM_011527988.2:c.1610+96_1610+99del	XP_011526290.2:n.1610+96_1610+99del
XM_011527989.3:c.1610+96_1610+99del	XP_011526291.2:n.1610+96_1610+99del
NM_000208.4:c.1610+96_1610+99del MANE Select	NP_000199.2:n.1610+96_1610+99del
NM_001079817.3:c.1610+96_1610+99del	NP_001073285.1:n.1610+96_1610+99del