Canonical Allele Identifier: CA403666668

Gene: INSR

Linked Data

• gnomAD v4: 19-7166378-T-A
• MyVariant Identifiers: chr19:g.7166389T>A (hg19) ; chr19:g.7166378T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166378T>A , CM000681.2:g.7166378T>A	GRCh38
NC_000019.9:g.7166389T>A , CM000681.1:g.7166389T>A	GRCh37
NC_000019.8:g.7117389T>A	NCBI36
NG_008852.2:g.132623A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.1637A>T MANE Select	ENSP00000303830.4:p.Asp546Val
ENST00000302850.9:c.1637A>T	ENSP00000303830.4:p.Asp546Val
ENST00000341500.9:c.1637A>T	ENSP00000342838.4:p.Asp546Val
ENST00000598216.1:n.1612A>T
ENST00000600492.1:c.38A>T	ENSP00000473170.1:p.Asp13Val
NM_000208.2:c.1637A>T	NP_000199.2:p.Asp546Val
NM_000208.3:c.1637A>T	NP_000199.2:p.Asp546Val
NM_001079817.1:c.1637A>T	NP_001073285.1:p.Asp546Val
NM_001079817.2:c.1637A>T	NP_001073285.1:p.Asp546Val
XM_011527988.1:c.1715A>T	XP_011526290.1:p.Asp572Val
XM_011527989.1:c.1715A>T	XP_011526291.1:p.Asp572Val
XM_011527988.2:c.1637A>T	XP_011526290.2:p.Asp546Val
XM_011527989.3:c.1637A>T	XP_011526291.2:p.Asp546Val
NM_000208.4:c.1637A>T MANE Select	NP_000199.2:p.Asp546Val
NM_001079817.3:c.1637A>T	NP_001073285.1:p.Asp546Val