Canonical Allele Identifier: CA2587925120

Gene: INSR

Linked Data

• gnomAD v4: 19-7166027-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166027C>G , CM000681.2:g.7166027C>G	GRCh38
NC_000019.9:g.7166038C>G , CM000681.1:g.7166038C>G	GRCh37
NC_000019.8:g.7117038C>G	NCBI36
NG_008852.2:g.132974G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1861+127G>C MANE Select	ENSP00000303830.4:n.1861+127G>C
ENST00000302850.9:c.1861+127G>C	ENSP00000303830.4:n.1861+127G>C
ENST00000341500.9:c.1861+127G>C	ENSP00000342838.4:n.1861+127G>C
ENST00000598216.1:n.1836+127G>C
ENST00000600492.1:c.262+127G>C	ENSP00000473170.1:n.262+127G>C
NM_000208.2:c.1861+127G>C	NP_000199.2:n.1861+127G>C
NM_000208.3:c.1861+127G>C	NP_000199.2:n.1861+127G>C
NM_001079817.1:c.1861+127G>C	NP_001073285.1:n.1861+127G>C
NM_001079817.2:c.1861+127G>C	NP_001073285.1:n.1861+127G>C
XM_011527988.1:c.1939+127G>C	XP_011526290.1:n.1939+127G>C
XM_011527989.1:c.1939+127G>C	XP_011526291.1:n.1939+127G>C
XM_011527988.2:c.1861+127G>C	XP_011526290.2:n.1861+127G>C
XM_011527989.3:c.1861+127G>C	XP_011526291.2:n.1861+127G>C
NM_000208.4:c.1861+127G>C MANE Select	NP_000199.2:n.1861+127G>C
NM_001079817.3:c.1861+127G>C	NP_001073285.1:n.1861+127G>C