Canonical Allele Identifier: CA403671685

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128875A>G (hg19) ; chr19:g.7128864A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128864A>G , CM000681.2:g.7128864A>G	GRCh38
NC_000019.9:g.7128875A>G , CM000681.1:g.7128875A>G	GRCh37
NC_000019.8:g.7079875A>G	NCBI36
NG_008852.2:g.170137T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2933T>C MANE Select	ENSP00000303830.4:p.Phe978Ser
ENST00000302850.9:c.2933T>C	ENSP00000303830.4:p.Phe978Ser
ENST00000341500.9:c.2897T>C	ENSP00000342838.4:p.Phe966Ser
NM_000208.2:c.2933T>C	NP_000199.2:p.Phe978Ser
NM_000208.3:c.2933T>C	NP_000199.2:p.Phe978Ser
NM_001079817.1:c.2897T>C	NP_001073285.1:p.Phe966Ser
NM_001079817.2:c.2897T>C	NP_001073285.1:p.Phe966Ser
XM_011527988.1:c.3008T>C	XP_011526290.1:p.Phe1003Ser
XM_011527989.1:c.2972T>C	XP_011526291.1:p.Phe991Ser
XM_011527988.2:c.2930T>C	XP_011526290.2:p.Phe977Ser
XM_011527989.3:c.2894T>C	XP_011526291.2:p.Phe965Ser
NM_000208.4:c.2933T>C MANE Select	NP_000199.2:p.Phe978Ser
NM_001079817.3:c.2897T>C	NP_001073285.1:p.Phe966Ser