Canonical Allele Identifier: CA403661649

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7141711T>A (hg19) ; chr19:g.7141700T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7141700T>A , CM000681.2:g.7141700T>A	GRCh38
NC_000019.9:g.7141711T>A , CM000681.1:g.7141711T>A	GRCh37
NC_000019.8:g.7092711T>A	NCBI36
NG_008852.2:g.157301A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2659A>T MANE Select	ENSP00000303830.4:p.Ser887Cys
ENST00000302850.9:c.2659A>T	ENSP00000303830.4:p.Ser887Cys
ENST00000341500.9:c.2623A>T	ENSP00000342838.4:p.Ser875Cys
ENST00000597211.1:n.342A>T
NM_000208.2:c.2659A>T	NP_000199.2:p.Ser887Cys
NM_000208.3:c.2659A>T	NP_000199.2:p.Ser887Cys
NM_001079817.1:c.2623A>T	NP_001073285.1:p.Ser875Cys
NM_001079817.2:c.2623A>T	NP_001073285.1:p.Ser875Cys
XM_011527988.1:c.2737A>T	XP_011526290.1:p.Ser913Cys
XM_011527989.1:c.2701A>T	XP_011526291.1:p.Ser901Cys
XM_011527988.2:c.2659A>T	XP_011526290.2:p.Ser887Cys
XM_011527989.3:c.2623A>T	XP_011526291.2:p.Ser875Cys
NM_000208.4:c.2659A>T MANE Select	NP_000199.2:p.Ser887Cys
NM_001079817.3:c.2623A>T	NP_001073285.1:p.Ser875Cys