Canonical Allele Identifier: CA631693682

Gene: INSR

Linked Data

• dbSNP Id: rs1371281026
• gnomAD v2: 19-7129001-A-G
• gnomAD v3: 19-7128990-A-G
• gnomAD v4: 19-7128990-A-G
• MyVariant Identifiers: chr19:g.7129001A>G (hg19) ; chr19:g.7128990A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128990A>G , CM000681.2:g.7128990A>G	GRCh38
NC_000019.9:g.7129001A>G , CM000681.1:g.7129001A>G	GRCh37
NC_000019.8:g.7080001A>G	NCBI36
NG_008852.2:g.170011T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2843-36T>C MANE Select	ENSP00000303830.4:n.2843-36T>C
ENST00000302850.9:c.2843-36T>C	ENSP00000303830.4:n.2843-36T>C
ENST00000341500.9:c.2807-36T>C	ENSP00000342838.4:n.2807-36T>C
NM_000208.2:c.2843-36T>C	NP_000199.2:n.2843-36T>C
NM_000208.3:c.2843-36T>C	NP_000199.2:n.2843-36T>C
NM_001079817.1:c.2807-36T>C	NP_001073285.1:n.2807-36T>C
NM_001079817.2:c.2807-36T>C	NP_001073285.1:n.2807-36T>C
XM_011527988.1:c.2921-39T>C	XP_011526290.1:n.2921-39T>C
XM_011527989.1:c.2885-39T>C	XP_011526291.1:n.2885-39T>C
XM_011527988.2:c.2843-39T>C	XP_011526290.2:n.2843-39T>C
XM_011527989.3:c.2807-39T>C	XP_011526291.2:n.2807-39T>C
NM_000208.4:c.2843-36T>C MANE Select	NP_000199.2:n.2843-36T>C
NM_001079817.3:c.2807-36T>C	NP_001073285.1:n.2807-36T>C