Canonical Allele Identifier: CA993114330

Gene: INSR

Linked Data

• dbSNP Id: rs1973999006
• gnomAD v3: 19-7170769-A-AT
• gnomAD v4: 19-7170769-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7170769_7170770insT , CM000681.2:g.7170769_7170770insT	GRCh38
NC_000019.9:g.7170780_7170781insT , CM000681.1:g.7170780_7170781insT	GRCh37
NC_000019.8:g.7121780_7121781insT	NCBI36
NG_008852.2:g.128231_128232insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1269-19_1269-18insA MANE Select	ENSP00000303830.4:n.1269-19_1269-18insA
ENST00000302850.9:c.1269-19_1269-18insA	ENSP00000303830.4:n.1269-19_1269-18insA
ENST00000341500.9:c.1269-19_1269-18insA	ENSP00000342838.4:n.1269-19_1269-18insA
ENST00000598216.1:n.1244-19_1244-18insA
NM_000208.2:c.1269-19_1269-18insA	NP_000199.2:n.1269-19_1269-18insA
NM_000208.3:c.1269-19_1269-18insA	NP_000199.2:n.1269-19_1269-18insA
NM_001079817.1:c.1269-19_1269-18insA	NP_001073285.1:n.1269-19_1269-18insA
NM_001079817.2:c.1269-19_1269-18insA	NP_001073285.1:n.1269-19_1269-18insA
XM_011527988.1:c.1347-19_1347-18insA	XP_011526290.1:n.1347-19_1347-18insA
XM_011527989.1:c.1347-19_1347-18insA	XP_011526291.1:n.1347-19_1347-18insA
XM_011527988.2:c.1269-19_1269-18insA	XP_011526290.2:n.1269-19_1269-18insA
XM_011527989.3:c.1269-19_1269-18insA	XP_011526291.2:n.1269-19_1269-18insA
NM_000208.4:c.1269-19_1269-18insA MANE Select	NP_000199.2:n.1269-19_1269-18insA
NM_001079817.3:c.1269-19_1269-18insA	NP_001073285.1:n.1269-19_1269-18insA