Canonical Allele Identifier: CA403669305

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7119596T>C (hg19) ; chr19:g.7119585T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7119585T>C , CM000681.2:g.7119585T>C	GRCh38
NC_000019.9:g.7119596T>C , CM000681.1:g.7119596T>C	GRCh37
NC_000019.8:g.7070596T>C	NCBI36
NG_008852.2:g.179416A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3660-2A>G MANE Select	ENSP00000303830.4:n.3660-2A>G
ENST00000302850.9:c.3660-2A>G	ENSP00000303830.4:n.3660-2A>G
ENST00000341500.9:c.3624-2A>G	ENSP00000342838.4:n.3624-2A>G
NM_000208.2:c.3660-2A>G	NP_000199.2:n.3660-2A>G
NM_000208.3:c.3660-2A>G	NP_000199.2:n.3660-2A>G
NM_001079817.1:c.3624-2A>G	NP_001073285.1:n.3624-2A>G
NM_001079817.2:c.3624-2A>G	NP_001073285.1:n.3624-2A>G
XM_011527988.1:c.3735-2A>G	XP_011526290.1:n.3735-2A>G
XM_011527989.1:c.3699-2A>G	XP_011526291.1:n.3699-2A>G
XM_011527988.2:c.3657-2A>G	XP_011526290.2:n.3657-2A>G
XM_011527989.3:c.3621-2A>G	XP_011526291.2:n.3621-2A>G
NM_000208.4:c.3660-2A>G MANE Select	NP_000199.2:n.3660-2A>G
NM_001079817.3:c.3624-2A>G	NP_001073285.1:n.3624-2A>G