Canonical Allele Identifier: CA2587926196
Gene: INSR HGNC NCBI

Linked Data

gnomAD v4: 19-7184288-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7184288G>T , CM000681.2:g.7184288G>T GRCh38
NC_000019.9:g.7184299G>T , CM000681.1:g.7184299G>T GRCh37
NC_000019.8:g.7135299G>T NCBI36
NG_008852.2:g.114713C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.974+28C>A MANE Select ENSP00000303830.4:n.974+28C>A
ENST00000302850.9:c.974+28C>A ENSP00000303830.4:n.974+28C>A
ENST00000341500.9:c.974+28C>A ENSP00000342838.4:n.974+28C>A
ENST00000598216.1:n.949+28C>A
NM_000208.2:c.974+28C>A NP_000199.2:n.974+28C>A
NM_000208.3:c.974+28C>A NP_000199.2:n.974+28C>A
NM_001079817.1:c.974+28C>A NP_001073285.1:n.974+28C>A
NM_001079817.2:c.974+28C>A NP_001073285.1:n.974+28C>A
XM_011527988.1:c.1052+28C>A XP_011526290.1:n.1052+28C>A
XM_011527989.1:c.1052+28C>A XP_011526291.1:n.1052+28C>A
XM_011527988.2:c.974+28C>A XP_011526290.2:n.974+28C>A
XM_011527989.3:c.974+28C>A XP_011526291.2:n.974+28C>A
NM_000208.4:c.974+28C>A MANE Select NP_000199.2:n.974+28C>A
NM_001079817.3:c.974+28C>A NP_001073285.1:n.974+28C>A
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