Canonical Allele Identifier: CA884174895

Gene: INSR

Linked Data

• dbSNP Id: rs1407142987
• gnomAD v3: 19-7116793-C-G
• gnomAD v4: 19-7116793-C-G
• MyVariant Identifiers: chr19:g.7116804C>G (hg19) ; chr19:g.7116793C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116793C>G , CM000681.2:g.7116793C>G	GRCh38
NC_000019.9:g.7116804C>G , CM000681.1:g.7116804C>G	GRCh37
NC_000019.8:g.7067804C>G	NCBI36
NG_008852.2:g.182208G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.*263G>C MANE Select	ENSP00000303830.4:n.*263G>C
ENST00000302850.9:c.*263G>C	ENSP00000303830.4:n.*263G>C
ENST00000341500.9:c.*263G>C	ENSP00000342838.4:n.*263G>C
NM_000208.2:c.*263G>C	NP_000199.2:n.*263G>C
NM_000208.3:c.*263G>C	NP_000199.2:n.*263G>C
NM_001079817.1:c.*263G>C	NP_001073285.1:n.*263G>C
NM_001079817.2:c.*263G>C	NP_001073285.1:n.*263G>C
XM_011527988.1:c.*263G>C	XP_011526290.1:n.*263G>C
XM_011527989.1:c.*263G>C	XP_011526291.1:n.*263G>C
XM_011527988.2:c.*263G>C	XP_011526290.2:n.*263G>C
XM_011527989.3:c.*263G>C	XP_011526291.2:n.*263G>C
NM_000208.4:c.*263G>C MANE Select	NP_000199.2:n.*263G>C
NM_001079817.3:c.*263G>C	NP_001073285.1:n.*263G>C