Canonical Allele Identifier: CA9135270

Gene: INSR

Linked Data

• dbSNP Id: rs747377285
• ExAC: 19:7122810 T / A
• gnomAD v2: 19-7122810-T-A
• gnomAD v4: 19-7122799-T-A
• MyVariant Identifiers: chr19:g.7122810T>A (hg19) ; chr19:g.7122799T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122799T>A , CM000681.2:g.7122799T>A	GRCh38
NC_000019.9:g.7122810T>A , CM000681.1:g.7122810T>A	GRCh37
NC_000019.8:g.7073810T>A	NCBI36
NG_008852.2:g.176202A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3370-26A>T MANE Select	ENSP00000303830.4:n.3370-26A>T
ENST00000302850.9:c.3370-26A>T	ENSP00000303830.4:n.3370-26A>T
ENST00000341500.9:c.3334-26A>T	ENSP00000342838.4:n.3334-26A>T
ENST00000593970.1:n.216-26A>T
ENST00000601099.1:n.281-26A>T
NM_000208.2:c.3370-26A>T	NP_000199.2:n.3370-26A>T
NM_000208.3:c.3370-26A>T	NP_000199.2:n.3370-26A>T
NM_001079817.1:c.3334-26A>T	NP_001073285.1:n.3334-26A>T
NM_001079817.2:c.3334-26A>T	NP_001073285.1:n.3334-26A>T
XM_011527988.1:c.3445-26A>T	XP_011526290.1:n.3445-26A>T
XM_011527989.1:c.3409-26A>T	XP_011526291.1:n.3409-26A>T
XM_011527988.2:c.3367-26A>T	XP_011526290.2:n.3367-26A>T
XM_011527989.3:c.3331-26A>T	XP_011526291.2:n.3331-26A>T
NM_000208.4:c.3370-26A>T MANE Select	NP_000199.2:n.3370-26A>T
NM_001079817.3:c.3334-26A>T	NP_001073285.1:n.3334-26A>T