Canonical Allele Identifier: CA403671088

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125347T>G (hg19) ; chr19:g.7125336T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125336T>G , CM000681.2:g.7125336T>G	GRCh38
NC_000019.9:g.7125347T>G , CM000681.1:g.7125347T>G	GRCh37
NC_000019.8:g.7076347T>G	NCBI36
NG_008852.2:g.173665A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3205A>C MANE Select	ENSP00000303830.4:p.Ile1069Leu
ENST00000302850.9:c.3205A>C	ENSP00000303830.4:p.Ile1069Leu
ENST00000341500.9:c.3169A>C	ENSP00000342838.4:p.Ile1057Leu
ENST00000593970.1:n.51A>C
NM_000208.2:c.3205A>C	NP_000199.2:p.Ile1069Leu
NM_000208.3:c.3205A>C	NP_000199.2:p.Ile1069Leu
NM_001079817.1:c.3169A>C	NP_001073285.1:p.Ile1057Leu
NM_001079817.2:c.3169A>C	NP_001073285.1:p.Ile1057Leu
XM_011527988.1:c.3280A>C	XP_011526290.1:p.Ile1094Leu
XM_011527989.1:c.3244A>C	XP_011526291.1:p.Ile1082Leu
XM_011527988.2:c.3202A>C	XP_011526290.2:p.Ile1068Leu
XM_011527989.3:c.3166A>C	XP_011526291.2:p.Ile1056Leu
NM_000208.4:c.3205A>C MANE Select	NP_000199.2:p.Ile1069Leu
NM_001079817.3:c.3169A>C	NP_001073285.1:p.Ile1057Leu