Canonical Allele Identifier: CA2537064342

Gene: INSR

Linked Data

• gnomAD v4: 19-7116967-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116967T>G , CM000681.2:g.7116967T>G	GRCh38
NC_000019.9:g.7116978T>G , CM000681.1:g.7116978T>G	GRCh37
NC_000019.8:g.7067978T>G	NCBI36
NG_008852.2:g.182034A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.*89A>C MANE Select	ENSP00000303830.4:n.*89A>C
ENST00000302850.9:c.*89A>C	ENSP00000303830.4:n.*89A>C
ENST00000341500.9:c.*89A>C	ENSP00000342838.4:n.*89A>C
NM_000208.2:c.*89A>C	NP_000199.2:n.*89A>C
NM_000208.3:c.*89A>C	NP_000199.2:n.*89A>C
NM_001079817.1:c.*89A>C	NP_001073285.1:n.*89A>C
NM_001079817.2:c.*89A>C	NP_001073285.1:n.*89A>C
XM_011527988.1:c.*89A>C	XP_011526290.1:n.*89A>C
XM_011527989.1:c.*89A>C	XP_011526291.1:n.*89A>C
XM_011527988.2:c.*89A>C	XP_011526290.2:n.*89A>C
XM_011527989.3:c.*89A>C	XP_011526291.2:n.*89A>C
NM_000208.4:c.*89A>C MANE Select	NP_000199.2:n.*89A>C
NM_001079817.3:c.*89A>C	NP_001073285.1:n.*89A>C