Canonical Allele Identifier: CA884176622

Gene: INSR

Linked Data

• dbSNP Id: rs1293238946
• MyVariant Identifiers: chr19:g.7125727T>C (hg19) ; chr19:g.7125716T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125716T>C , CM000681.2:g.7125716T>C	GRCh38
NC_000019.9:g.7125727T>C , CM000681.1:g.7125727T>C	GRCh37
NC_000019.8:g.7076727T>C	NCBI36
NG_008852.2:g.173285A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3014-189A>G MANE Select	ENSP00000303830.4:n.3014-189A>G
ENST00000302850.9:c.3014-189A>G	ENSP00000303830.4:n.3014-189A>G
ENST00000341500.9:c.2978-189A>G	ENSP00000342838.4:n.2978-189A>G
NM_000208.2:c.3014-189A>G	NP_000199.2:n.3014-189A>G
NM_000208.3:c.3014-189A>G	NP_000199.2:n.3014-189A>G
NM_001079817.1:c.2978-189A>G	NP_001073285.1:n.2978-189A>G
NM_001079817.2:c.2978-189A>G	NP_001073285.1:n.2978-189A>G
XM_011527988.1:c.3089-189A>G	XP_011526290.1:n.3089-189A>G
XM_011527989.1:c.3053-189A>G	XP_011526291.1:n.3053-189A>G
XM_011527988.2:c.3011-189A>G	XP_011526290.2:n.3011-189A>G
XM_011527989.3:c.2975-189A>G	XP_011526291.2:n.2975-189A>G
NM_000208.4:c.3014-189A>G MANE Select	NP_000199.2:n.3014-189A>G
NM_001079817.3:c.2978-189A>G	NP_001073285.1:n.2978-189A>G