Canonical Allele Identifier: CA304842331

Gene: INSR

Linked Data

• dbSNP Id: rs931617081
• MyVariant Identifiers: chr19:g.7150336A>G (hg19) ; chr19:g.7150325A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7150325A>G , CM000681.2:g.7150325A>G	GRCh38
NC_000019.9:g.7150336A>G , CM000681.1:g.7150336A>G	GRCh37
NC_000019.8:g.7101336A>G	NCBI36
NG_008852.2:g.148676T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2267+172T>C MANE Select	ENSP00000303830.4:n.2267+172T>C
ENST00000302850.9:c.2267+172T>C	ENSP00000303830.4:n.2267+172T>C
ENST00000341500.9:c.2231+2401T>C	ENSP00000342838.4:n.2231+2401T>C
NM_000208.2:c.2267+172T>C	NP_000199.2:n.2267+172T>C
NM_000208.3:c.2267+172T>C	NP_000199.2:n.2267+172T>C
NM_001079817.1:c.2231+2401T>C	NP_001073285.1:n.2231+2401T>C
NM_001079817.2:c.2231+2401T>C	NP_001073285.1:n.2231+2401T>C
XM_011527988.1:c.2345+172T>C	XP_011526290.1:n.2345+172T>C
XM_011527989.1:c.2309+2401T>C	XP_011526291.1:n.2309+2401T>C
XM_011527988.2:c.2267+172T>C	XP_011526290.2:n.2267+172T>C
XM_011527989.3:c.2231+2401T>C	XP_011526291.2:n.2231+2401T>C
NM_000208.4:c.2267+172T>C MANE Select	NP_000199.2:n.2267+172T>C
NM_001079817.3:c.2231+2401T>C	NP_001073285.1:n.2231+2401T>C