Canonical Allele Identifier: CA884186405

Gene: INSR

Linked Data

• dbSNP Id: rs1318745696
• MyVariant Identifiers: chr19:g.7150295G>A (hg19) ; chr19:g.7150284G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7150284G>A , CM000681.2:g.7150284G>A	GRCh38
NC_000019.9:g.7150295G>A , CM000681.1:g.7150295G>A	GRCh37
NC_000019.8:g.7101295G>A	NCBI36
NG_008852.2:g.148717C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2267+213C>T MANE Select	ENSP00000303830.4:n.2267+213C>T
ENST00000302850.9:c.2267+213C>T	ENSP00000303830.4:n.2267+213C>T
ENST00000341500.9:c.2231+2442C>T	ENSP00000342838.4:n.2231+2442C>T
NM_000208.2:c.2267+213C>T	NP_000199.2:n.2267+213C>T
NM_000208.3:c.2267+213C>T	NP_000199.2:n.2267+213C>T
NM_001079817.1:c.2231+2442C>T	NP_001073285.1:n.2231+2442C>T
NM_001079817.2:c.2231+2442C>T	NP_001073285.1:n.2231+2442C>T
XM_011527988.1:c.2345+213C>T	XP_011526290.1:n.2345+213C>T
XM_011527989.1:c.2309+2442C>T	XP_011526291.1:n.2309+2442C>T
XM_011527988.2:c.2267+213C>T	XP_011526290.2:n.2267+213C>T
XM_011527989.3:c.2231+2442C>T	XP_011526291.2:n.2231+2442C>T
NM_000208.4:c.2267+213C>T MANE Select	NP_000199.2:n.2267+213C>T
NM_001079817.3:c.2231+2442C>T	NP_001073285.1:n.2231+2442C>T