Canonical Allele Identifier: CA403671294

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7125444C>T (hg19) ; chr19:g.7125433C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125433C>T , CM000681.2:g.7125433C>T	GRCh38
NC_000019.9:g.7125444C>T , CM000681.1:g.7125444C>T	GRCh37
NC_000019.8:g.7076444C>T	NCBI36
NG_008852.2:g.173568G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3108G>A MANE Select	ENSP00000303830.4:p.Met1036Ile
ENST00000302850.9:c.3108G>A	ENSP00000303830.4:p.Met1036Ile
ENST00000341500.9:c.3072G>A	ENSP00000342838.4:p.Met1024Ile
NM_000208.2:c.3108G>A	NP_000199.2:p.Met1036Ile
NM_000208.3:c.3108G>A	NP_000199.2:p.Met1036Ile
NM_001079817.1:c.3072G>A	NP_001073285.1:p.Met1024Ile
NM_001079817.2:c.3072G>A	NP_001073285.1:p.Met1024Ile
XM_011527988.1:c.3183G>A	XP_011526290.1:p.Met1061Ile
XM_011527989.1:c.3147G>A	XP_011526291.1:p.Met1049Ile
XM_011527988.2:c.3105G>A	XP_011526290.2:p.Met1035Ile
XM_011527989.3:c.3069G>A	XP_011526291.2:p.Met1023Ile
NM_000208.4:c.3108G>A MANE Select	NP_000199.2:p.Met1036Ile
NM_001079817.3:c.3072G>A	NP_001073285.1:p.Met1024Ile