Canonical Allele Identifier: CA403666445

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7166288T>A (hg19) ; chr19:g.7166277T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166277T>A , CM000681.2:g.7166277T>A	GRCh38
NC_000019.9:g.7166288T>A , CM000681.1:g.7166288T>A	GRCh37
NC_000019.8:g.7117288T>A	NCBI36
NG_008852.2:g.132724A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.1738A>T MANE Select	ENSP00000303830.4:p.Met580Leu
ENST00000302850.9:c.1738A>T	ENSP00000303830.4:p.Met580Leu
ENST00000341500.9:c.1738A>T	ENSP00000342838.4:p.Met580Leu
ENST00000598216.1:n.1713A>T
ENST00000600492.1:c.139A>T	ENSP00000473170.1:p.Met47Leu
NM_000208.2:c.1738A>T	NP_000199.2:p.Met580Leu
NM_000208.3:c.1738A>T	NP_000199.2:p.Met580Leu
NM_001079817.1:c.1738A>T	NP_001073285.1:p.Met580Leu
NM_001079817.2:c.1738A>T	NP_001073285.1:p.Met580Leu
XM_011527988.1:c.1816A>T	XP_011526290.1:p.Met606Leu
XM_011527989.1:c.1816A>T	XP_011526291.1:p.Met606Leu
XM_011527988.2:c.1738A>T	XP_011526290.2:p.Met580Leu
XM_011527989.3:c.1738A>T	XP_011526291.2:p.Met580Leu
NM_000208.4:c.1738A>T MANE Select	NP_000199.2:p.Met580Leu
NM_001079817.3:c.1738A>T	NP_001073285.1:p.Met580Leu