Canonical Allele Identifier: CA2587925706

Gene: INSR

Linked Data

• gnomAD v4: 19-7170771-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7170771A>G , CM000681.2:g.7170771A>G	GRCh38
NC_000019.9:g.7170782A>G , CM000681.1:g.7170782A>G	GRCh37
NC_000019.8:g.7121782A>G	NCBI36
NG_008852.2:g.128230T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1269-20T>C MANE Select	ENSP00000303830.4:n.1269-20T>C
ENST00000302850.9:c.1269-20T>C	ENSP00000303830.4:n.1269-20T>C
ENST00000341500.9:c.1269-20T>C	ENSP00000342838.4:n.1269-20T>C
ENST00000598216.1:n.1244-20T>C
NM_000208.2:c.1269-20T>C	NP_000199.2:n.1269-20T>C
NM_000208.3:c.1269-20T>C	NP_000199.2:n.1269-20T>C
NM_001079817.1:c.1269-20T>C	NP_001073285.1:n.1269-20T>C
NM_001079817.2:c.1269-20T>C	NP_001073285.1:n.1269-20T>C
XM_011527988.1:c.1347-20T>C	XP_011526290.1:n.1347-20T>C
XM_011527989.1:c.1347-20T>C	XP_011526291.1:n.1347-20T>C
XM_011527988.2:c.1269-20T>C	XP_011526290.2:n.1269-20T>C
XM_011527989.3:c.1269-20T>C	XP_011526291.2:n.1269-20T>C
NM_000208.4:c.1269-20T>C MANE Select	NP_000199.2:n.1269-20T>C
NM_001079817.3:c.1269-20T>C	NP_001073285.1:n.1269-20T>C