Canonical Allele Identifier: CA505217364

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7128871C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128860C>A , CM000681.2:g.7128860C>A	GRCh38
NC_000019.9:g.7128871C>A , CM000681.1:g.7128871C>A	GRCh37
NC_000019.8:g.7079871C>A	NCBI36
NG_008852.2:g.170141G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2937G>T MANE Select	ENSP00000303830.4:p.Leu979=
ENST00000302850.9:c.2937G>T	ENSP00000303830.4:p.Leu979=
ENST00000341500.9:c.2901G>T	ENSP00000342838.4:p.Leu967=
NM_000208.2:c.2937G>T	NP_000199.2:p.Leu979=
NM_000208.3:c.2937G>T	NP_000199.2:p.Leu979=
NM_001079817.1:c.2901G>T	NP_001073285.1:p.Leu967=
NM_001079817.2:c.2901G>T	NP_001073285.1:p.Leu967=
XM_011527988.1:c.3012G>T	XP_011526290.1:p.Leu1004=
XM_011527989.1:c.2976G>T	XP_011526291.1:p.Leu992=
XM_011527988.2:c.2934G>T	XP_011526290.2:p.Leu978=
XM_011527989.3:c.2898G>T	XP_011526291.2:p.Leu966=
NM_000208.4:c.2937G>T MANE Select	NP_000199.2:p.Leu979=
NM_001079817.3:c.2901G>T	NP_001073285.1:p.Leu967=