Canonical Allele Identifier: CA2587923169

Gene: INSR

Linked Data

• gnomAD v4: 19-7150345-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7150345G>T , CM000681.2:g.7150345G>T	GRCh38
NC_000019.9:g.7150356G>T , CM000681.1:g.7150356G>T	GRCh37
NC_000019.8:g.7101356G>T	NCBI36
NG_008852.2:g.148656C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2267+152C>A MANE Select	ENSP00000303830.4:n.2267+152C>A
ENST00000302850.9:c.2267+152C>A	ENSP00000303830.4:n.2267+152C>A
ENST00000341500.9:c.2231+2381C>A	ENSP00000342838.4:n.2231+2381C>A
NM_000208.2:c.2267+152C>A	NP_000199.2:n.2267+152C>A
NM_000208.3:c.2267+152C>A	NP_000199.2:n.2267+152C>A
NM_001079817.1:c.2231+2381C>A	NP_001073285.1:n.2231+2381C>A
NM_001079817.2:c.2231+2381C>A	NP_001073285.1:n.2231+2381C>A
XM_011527988.1:c.2345+152C>A	XP_011526290.1:n.2345+152C>A
XM_011527989.1:c.2309+2381C>A	XP_011526291.1:n.2309+2381C>A
XM_011527988.2:c.2267+152C>A	XP_011526290.2:n.2267+152C>A
XM_011527989.3:c.2231+2381C>A	XP_011526291.2:n.2231+2381C>A
NM_000208.4:c.2267+152C>A MANE Select	NP_000199.2:n.2267+152C>A
NM_001079817.3:c.2231+2381C>A	NP_001073285.1:n.2231+2381C>A