Canonical Allele Identifier: CA2320763763

Gene: INSR

Linked Data

• dbSNP Id: rs1040321803

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116852A>G , CM000681.2:g.7116852A>G	GRCh38
NC_000019.9:g.7116863A>G , CM000681.1:g.7116863A>G	GRCh37
NC_000019.8:g.7067863A>G	NCBI36
NG_008852.2:g.182149T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.*204T>C MANE Select	ENSP00000303830.4:n.*204T>C
ENST00000302850.9:c.*204T>C	ENSP00000303830.4:n.*204T>C
ENST00000341500.9:c.*204T>C	ENSP00000342838.4:n.*204T>C
NM_000208.2:c.*204T>C	NP_000199.2:n.*204T>C
NM_000208.3:c.*204T>C	NP_000199.2:n.*204T>C
NM_001079817.1:c.*204T>C	NP_001073285.1:n.*204T>C
NM_001079817.2:c.*204T>C	NP_001073285.1:n.*204T>C
XM_011527988.1:c.*204T>C	XP_011526290.1:n.*204T>C
XM_011527989.1:c.*204T>C	XP_011526291.1:n.*204T>C
XM_011527988.2:c.*204T>C	XP_011526290.2:n.*204T>C
XM_011527989.3:c.*204T>C	XP_011526291.2:n.*204T>C
NM_000208.4:c.*204T>C MANE Select	NP_000199.2:n.*204T>C
NM_001079817.3:c.*204T>C	NP_001073285.1:n.*204T>C