Canonical Allele Identifier: CA403670854

Gene: INSR

Linked Data

• dbSNP Id: rs1203185545
• gnomAD v2: 19-7122951-A-G
• MyVariant Identifiers: chr19:g.7122951A>G (hg19) ; chr19:g.7122940A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122940A>G , CM000681.2:g.7122940A>G	GRCh38
NC_000019.9:g.7122951A>G , CM000681.1:g.7122951A>G	GRCh37
NC_000019.8:g.7073951A>G	NCBI36
NG_008852.2:g.176061T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3308T>C MANE Select	ENSP00000303830.4:p.Met1103Thr
ENST00000302850.9:c.3308T>C	ENSP00000303830.4:p.Met1103Thr
ENST00000341500.9:c.3272T>C	ENSP00000342838.4:p.Met1091Thr
ENST00000593970.1:n.154T>C
ENST00000601099.1:n.219T>C
NM_000208.2:c.3308T>C	NP_000199.2:p.Met1103Thr
NM_000208.3:c.3308T>C	NP_000199.2:p.Met1103Thr
NM_001079817.1:c.3272T>C	NP_001073285.1:p.Met1091Thr
NM_001079817.2:c.3272T>C	NP_001073285.1:p.Met1091Thr
XM_011527988.1:c.3383T>C	XP_011526290.1:p.Met1128Thr
XM_011527989.1:c.3347T>C	XP_011526291.1:p.Met1116Thr
XM_011527988.2:c.3305T>C	XP_011526290.2:p.Met1102Thr
XM_011527989.3:c.3269T>C	XP_011526291.2:p.Met1090Thr
NM_000208.4:c.3308T>C MANE Select	NP_000199.2:p.Met1103Thr
NM_001079817.3:c.3272T>C	NP_001073285.1:p.Met1091Thr