Canonical Allele Identifier: CA869019933

Gene: TRMO

Linked Data

• dbSNP Id: rs10984377
• MyVariant Identifiers: chr9:g.100684534A>C (hg19) ; chr9:g.97922252A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97922252A>C , CM000671.2:g.97922252A>C	GRCh38
NC_000009.11:g.100684534A>C , CM000671.1:g.100684534A>C	GRCh37
NC_000009.10:g.99724355A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375119.8:c.76+166T>G MANE Select	ENSP00000364260.3:n.76+166T>G
ENST00000375117.8:c.73+166T>G	ENSP00000364258.4:n.73+166T>G
ENST00000375119.7:c.76+166T>G	ENSP00000364260.3:n.76+166T>G
ENST00000455506.1:c.70+166T>G	ENSP00000408473.1:n.70+166T>G
ENST00000471580.1:n.51+166T>G
ENST00000478126.5:n.55+166T>G
ENST00000611338.4:c.-2340+166T>G	ENSP00000483071.1:n.-2340+166T>G
NM_016481.4:c.76+166T>G	NP_057565.3:n.76+166T>G
XM_005252047.3:c.76+166T>G	XP_005252104.1:n.76+166T>G
XM_005252048.3:c.-466+166T>G	XP_005252105.1:n.-466+166T>G
XM_005252049.3:c.-188+166T>G	XP_005252106.1:n.-188+166T>G
XM_005252050.3:c.-291+166T>G	XP_005252107.1:n.-291+166T>G
XM_011518776.1:c.76+166T>G	XP_011517078.1:n.76+166T>G
XM_011518777.1:c.-315+166T>G	XP_011517079.1:n.-315+166T>G
XR_929808.1:n.110+166T>G
XR_929809.1:n.110+166T>G
XR_929810.1:n.110+166T>G
NM_001330725.1:c.-466+166T>G	NP_001317654.1:n.-466+166T>G
XM_005252047.4:c.76+166T>G	XP_005252104.1:n.76+166T>G
XM_005252049.5:c.-188+166T>G	XP_005252106.1:n.-188+166T>G
XM_005252050.4:c.-291+166T>G	XP_005252107.1:n.-291+166T>G
XM_011518776.3:c.76+166T>G	XP_011517078.1:n.76+166T>G
XM_024447569.1:c.-2722+166T>G	XP_024303337.1:n.-2722+166T>G
XR_929808.3:n.132+166T>G
NM_001330725.2:c.-466+166T>G	NP_001317654.1:n.-466+166T>G
NM_001371657.1:c.76+166T>G	NP_001358586.1:n.76+166T>G
NM_001371658.1:c.76+166T>G	NP_001358587.1:n.76+166T>G
NM_001371660.1:c.-291+166T>G	NP_001358589.1:n.-291+166T>G
NM_001371661.1:c.-188+166T>G	NP_001358590.1:n.-188+166T>G
NM_016481.5:c.76+166T>G MANE Select	NP_057565.3:n.76+166T>G