Canonical Allele Identifier: CA631723646

Gene: INSR

Linked Data

• dbSNP Id: rs1467048345
• gnomAD v2: 19-7122820-A-G
• gnomAD v4: 19-7122809-A-G
• MyVariant Identifiers: chr19:g.7122820A>G (hg19) ; chr19:g.7122809A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122809A>G , CM000681.2:g.7122809A>G	GRCh38
NC_000019.9:g.7122820A>G , CM000681.1:g.7122820A>G	GRCh37
NC_000019.8:g.7073820A>G	NCBI36
NG_008852.2:g.176192T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3370-36T>C MANE Select	ENSP00000303830.4:n.3370-36T>C
ENST00000302850.9:c.3370-36T>C	ENSP00000303830.4:n.3370-36T>C
ENST00000341500.9:c.3334-36T>C	ENSP00000342838.4:n.3334-36T>C
ENST00000593970.1:n.216-36T>C
ENST00000601099.1:n.281-36T>C
NM_000208.2:c.3370-36T>C	NP_000199.2:n.3370-36T>C
NM_000208.3:c.3370-36T>C	NP_000199.2:n.3370-36T>C
NM_001079817.1:c.3334-36T>C	NP_001073285.1:n.3334-36T>C
NM_001079817.2:c.3334-36T>C	NP_001073285.1:n.3334-36T>C
XM_011527988.1:c.3445-36T>C	XP_011526290.1:n.3445-36T>C
XM_011527989.1:c.3409-36T>C	XP_011526291.1:n.3409-36T>C
XM_011527988.2:c.3367-36T>C	XP_011526290.2:n.3367-36T>C
XM_011527989.3:c.3331-36T>C	XP_011526291.2:n.3331-36T>C
NM_000208.4:c.3370-36T>C MANE Select	NP_000199.2:n.3370-36T>C
NM_001079817.3:c.3334-36T>C	NP_001073285.1:n.3334-36T>C