Canonical Allele Identifier: CA403669385

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7120663C>G (hg19) ; chr19:g.7120652C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120652C>G , CM000681.2:g.7120652C>G	GRCh38
NC_000019.9:g.7120663C>G , CM000681.1:g.7120663C>G	GRCh37
NC_000019.8:g.7071663C>G	NCBI36
NG_008852.2:g.178349G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3627G>C MANE Select	ENSP00000303830.4:p.Lys1209Asn
ENST00000302850.9:c.3627G>C	ENSP00000303830.4:p.Lys1209Asn
ENST00000341500.9:c.3591G>C	ENSP00000342838.4:p.Lys1197Asn
ENST00000601099.1:n.538G>C
NM_000208.2:c.3627G>C	NP_000199.2:p.Lys1209Asn
NM_000208.3:c.3627G>C	NP_000199.2:p.Lys1209Asn
NM_001079817.1:c.3591G>C	NP_001073285.1:p.Lys1197Asn
NM_001079817.2:c.3591G>C	NP_001073285.1:p.Lys1197Asn
XM_011527988.1:c.3702G>C	XP_011526290.1:p.Lys1234Asn
XM_011527989.1:c.3666G>C	XP_011526291.1:p.Lys1222Asn
XM_011527988.2:c.3624G>C	XP_011526290.2:p.Lys1208Asn
XM_011527989.3:c.3588G>C	XP_011526291.2:p.Lys1196Asn
NM_000208.4:c.3627G>C MANE Select	NP_000199.2:p.Lys1209Asn
NM_001079817.3:c.3591G>C	NP_001073285.1:p.Lys1197Asn