Canonical Allele Identifier: CA884174940

Gene: INSR

Linked Data

• dbSNP Id: rs1347444995
• gnomAD v3: 19-7116909-C-CT
• gnomAD v4: 19-7116909-C-CT
• MyVariant Identifiers: chr19:g.7116920_7116921insT (hg19) ; chr19:g.7116909_7116910insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116911dup , CM000681.2:g.7116911dup	GRCh38
NC_000019.9:g.7116922dup , CM000681.1:g.7116922dup	GRCh37
NC_000019.8:g.7067922dup	NCBI36
NG_008852.2:g.182091dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.*146dup MANE Select	ENSP00000303830.4:n.*146dup
ENST00000302850.9:c.*146dup	ENSP00000303830.4:n.*146dup
ENST00000341500.9:c.*146dup	ENSP00000342838.4:n.*146dup
NM_000208.2:c.*146dup	NP_000199.2:n.*146dup
NM_000208.3:c.*146dup	NP_000199.2:n.*146dup
NM_001079817.1:c.*146dup	NP_001073285.1:n.*146dup
NM_001079817.2:c.*146dup	NP_001073285.1:n.*146dup
XM_011527988.1:c.*146dup	XP_011526290.1:n.*146dup
XM_011527989.1:c.*146dup	XP_011526291.1:n.*146dup
XM_011527988.2:c.*146dup	XP_011526290.2:n.*146dup
XM_011527989.3:c.*146dup	XP_011526291.2:n.*146dup
NM_000208.4:c.*146dup MANE Select	NP_000199.2:n.*146dup
NM_001079817.3:c.*146dup	NP_001073285.1:n.*146dup