Canonical Allele Identifier: CA403670857

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7122952T>G (hg19) ; chr19:g.7122941T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122941T>G , CM000681.2:g.7122941T>G	GRCh38
NC_000019.9:g.7122952T>G , CM000681.1:g.7122952T>G	GRCh37
NC_000019.8:g.7073952T>G	NCBI36
NG_008852.2:g.176060A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3307A>C MANE Select	ENSP00000303830.4:p.Met1103Leu
ENST00000302850.9:c.3307A>C	ENSP00000303830.4:p.Met1103Leu
ENST00000341500.9:c.3271A>C	ENSP00000342838.4:p.Met1091Leu
ENST00000593970.1:n.153A>C
ENST00000601099.1:n.218A>C
NM_000208.2:c.3307A>C	NP_000199.2:p.Met1103Leu
NM_000208.3:c.3307A>C	NP_000199.2:p.Met1103Leu
NM_001079817.1:c.3271A>C	NP_001073285.1:p.Met1091Leu
NM_001079817.2:c.3271A>C	NP_001073285.1:p.Met1091Leu
XM_011527988.1:c.3382A>C	XP_011526290.1:p.Met1128Leu
XM_011527989.1:c.3346A>C	XP_011526291.1:p.Met1116Leu
XM_011527988.2:c.3304A>C	XP_011526290.2:p.Met1102Leu
XM_011527989.3:c.3268A>C	XP_011526291.2:p.Met1090Leu
NM_000208.4:c.3307A>C MANE Select	NP_000199.2:p.Met1103Leu
NM_001079817.3:c.3271A>C	NP_001073285.1:p.Met1091Leu