Canonical Allele Identifier: CA10652830

Gene: INSR

Linked Data

• ClinVar Variation Id: 330356
• ClinVar RCV Id: RCV000272374 ; RCV000301605 ; RCV000358785
• dbSNP Id: rs1366600
• gnomAD v2: 19-7112881-A-G
• gnomAD v3: 19-7112870-A-G
• gnomAD v4: 19-7112870-A-G
• MyVariant Identifiers: chr19:g.7112881A>G (hg19) ; chr19:g.7112870A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7112870A>G , CM000681.2:g.7112870A>G	GRCh38
NC_000019.9:g.7112881A>G , CM000681.1:g.7112881A>G	GRCh37
NC_000019.8:g.7063881A>G	NCBI36
NG_008852.2:g.186131T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.*4186T>C MANE Select	ENSP00000303830.4:n.*4186T>C
ENST00000341500.9:c.*4186T>C	ENSP00000342838.4:n.*4186T>C
NM_000208.2:c.*4186T>C	NP_000199.2:n.*4186T>C
NM_000208.3:c.*4186T>C	NP_000199.2:n.*4186T>C
NM_001079817.1:c.*4186T>C	NP_001073285.1:n.*4186T>C
NM_001079817.2:c.*4186T>C	NP_001073285.1:n.*4186T>C
XM_011527988.1:c.*4186T>C	XP_011526290.1:n.*4186T>C
XM_011527989.1:c.*4186T>C	XP_011526291.1:n.*4186T>C
XM_011527988.2:c.*4186T>C	XP_011526290.2:n.*4186T>C
XM_011527989.3:c.*4186T>C	XP_011526291.2:n.*4186T>C
NM_000208.4:c.*4186T>C MANE Select	NP_000199.2:n.*4186T>C
NM_001079817.3:c.*4186T>C	NP_001073285.1:n.*4186T>C