Canonical Allele Identifier: CA2587921709

Gene: INSR

Linked Data

• gnomAD v4: 19-7123031-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7123031A>G , CM000681.2:g.7123031A>G	GRCh38
NC_000019.9:g.7123042A>G , CM000681.1:g.7123042A>G	GRCh37
NC_000019.8:g.7074042A>G	NCBI36
NG_008852.2:g.175970T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3259-42T>C MANE Select	ENSP00000303830.4:n.3259-42T>C
ENST00000302850.9:c.3259-42T>C	ENSP00000303830.4:n.3259-42T>C
ENST00000341500.9:c.3223-42T>C	ENSP00000342838.4:n.3223-42T>C
ENST00000593970.1:n.105-42T>C
ENST00000601099.1:n.128T>C
NM_000208.2:c.3259-42T>C	NP_000199.2:n.3259-42T>C
NM_000208.3:c.3259-42T>C	NP_000199.2:n.3259-42T>C
NM_001079817.1:c.3223-42T>C	NP_001073285.1:n.3223-42T>C
NM_001079817.2:c.3223-42T>C	NP_001073285.1:n.3223-42T>C
XM_011527988.1:c.3334-42T>C	XP_011526290.1:n.3334-42T>C
XM_011527989.1:c.3298-42T>C	XP_011526291.1:n.3298-42T>C
XM_011527988.2:c.3256-42T>C	XP_011526290.2:n.3256-42T>C
XM_011527989.3:c.3220-42T>C	XP_011526291.2:n.3220-42T>C
NM_000208.4:c.3259-42T>C MANE Select	NP_000199.2:n.3259-42T>C
NM_001079817.3:c.3223-42T>C	NP_001073285.1:n.3223-42T>C