Canonical Allele Identifier: CA403668497

Gene: INSR

Linked Data

• gnomAD v4: 19-7117199-G-A
• MyVariant Identifiers: chr19:g.7117210G>A (hg19) ; chr19:g.7117199G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117199G>A , CM000681.2:g.7117199G>A	GRCh38
NC_000019.9:g.7117210G>A , CM000681.1:g.7117210G>A	GRCh37
NC_000019.8:g.7068210G>A	NCBI36
NG_008852.2:g.181802C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4006C>T MANE Select	ENSP00000303830.4:p.Gln1336Ter
ENST00000302850.9:c.4006C>T	ENSP00000303830.4:p.Gln1336Ter
ENST00000341500.9:c.3970C>T	ENSP00000342838.4:p.Gln1324Ter
NM_000208.2:c.4006C>T	NP_000199.2:p.Gln1336Ter
NM_000208.3:c.4006C>T	NP_000199.2:p.Gln1336Ter
NM_001079817.1:c.3970C>T	NP_001073285.1:p.Gln1324Ter
NM_001079817.2:c.3970C>T	NP_001073285.1:p.Gln1324Ter
XM_011527988.1:c.4081C>T	XP_011526290.1:p.Gln1361Ter
XM_011527989.1:c.4045C>T	XP_011526291.1:p.Gln1349Ter
XM_011527988.2:c.4003C>T	XP_011526290.2:p.Gln1335Ter
XM_011527989.3:c.3967C>T	XP_011526291.2:p.Gln1323Ter
NM_000208.4:c.4006C>T MANE Select	NP_000199.2:p.Gln1336Ter
NM_001079817.3:c.3970C>T	NP_001073285.1:p.Gln1324Ter