Canonical Allele Identifier: CA2587922080

Gene: INSR

Linked Data

• gnomAD v4: 19-7125257-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125257C>G , CM000681.2:g.7125257C>G	GRCh38
NC_000019.9:g.7125268C>G , CM000681.1:g.7125268C>G	GRCh37
NC_000019.8:g.7076268C>G	NCBI36
NG_008852.2:g.173744G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3258+26G>C MANE Select	ENSP00000303830.4:n.3258+26G>C
ENST00000302850.9:c.3258+26G>C	ENSP00000303830.4:n.3258+26G>C
ENST00000341500.9:c.3222+26G>C	ENSP00000342838.4:n.3222+26G>C
ENST00000593970.1:n.104+26G>C
NM_000208.2:c.3258+26G>C	NP_000199.2:n.3258+26G>C
NM_000208.3:c.3258+26G>C	NP_000199.2:n.3258+26G>C
NM_001079817.1:c.3222+26G>C	NP_001073285.1:n.3222+26G>C
NM_001079817.2:c.3222+26G>C	NP_001073285.1:n.3222+26G>C
XM_011527988.1:c.3333+26G>C	XP_011526290.1:n.3333+26G>C
XM_011527989.1:c.3297+26G>C	XP_011526291.1:n.3297+26G>C
XM_011527988.2:c.3255+26G>C	XP_011526290.2:n.3255+26G>C
XM_011527989.3:c.3219+26G>C	XP_011526291.2:n.3219+26G>C
NM_000208.4:c.3258+26G>C MANE Select	NP_000199.2:n.3258+26G>C
NM_001079817.3:c.3222+26G>C	NP_001073285.1:n.3222+26G>C