Canonical Allele Identifier: CA2320768125

Gene: INSR

Linked Data

• dbSNP Id: rs1972631711

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125743A>G , CM000681.2:g.7125743A>G	GRCh38
NC_000019.9:g.7125754A>G , CM000681.1:g.7125754A>G	GRCh37
NC_000019.8:g.7076754A>G	NCBI36
NG_008852.2:g.173258T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3014-216T>C MANE Select	ENSP00000303830.4:n.3014-216T>C
ENST00000302850.9:c.3014-216T>C	ENSP00000303830.4:n.3014-216T>C
ENST00000341500.9:c.2978-216T>C	ENSP00000342838.4:n.2978-216T>C
NM_000208.2:c.3014-216T>C	NP_000199.2:n.3014-216T>C
NM_000208.3:c.3014-216T>C	NP_000199.2:n.3014-216T>C
NM_001079817.1:c.2978-216T>C	NP_001073285.1:n.2978-216T>C
NM_001079817.2:c.2978-216T>C	NP_001073285.1:n.2978-216T>C
XM_011527988.1:c.3089-216T>C	XP_011526290.1:n.3089-216T>C
XM_011527989.1:c.3053-216T>C	XP_011526291.1:n.3053-216T>C
XM_011527988.2:c.3011-216T>C	XP_011526290.2:n.3011-216T>C
XM_011527989.3:c.2975-216T>C	XP_011526291.2:n.2975-216T>C
NM_000208.4:c.3014-216T>C MANE Select	NP_000199.2:n.3014-216T>C
NM_001079817.3:c.2978-216T>C	NP_001073285.1:n.2978-216T>C