Canonical Allele Identifier: CA204365

Gene: SIGMAR1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34637546C>A , CM000671.2:g.34637546C>A	GRCh38
NC_000009.11:g.34637543C>A , CM000671.1:g.34637543C>A	GRCh37
NC_000009.10:g.34627543C>A	NCBI36
NG_029945.2:g.5226G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000277010.9:c.151+1G>T MANE Select	ENSP00000277010.4:n.151+1G>T
ENST00000497006.2:n.298+1G>T
ENST00000679597.1:c.91+61G>T	ENSP00000505634.1:n.91+61G>T
ENST00000680104.1:c.151+1G>T	ENSP00000505949.1:n.151+1G>T
ENST00000680244.1:c.151+1G>T	ENSP00000505305.1:n.151+1G>T
ENST00000680277.1:c.151+1G>T	ENSP00000505742.1:n.151+1G>T
ENST00000680730.1:c.151+1G>T	ENSP00000505588.1:n.151+1G>T
ENST00000681409.1:n.270+1G>T
ENST00000277010.8:c.151+1G>T	ENSP00000277010.4:n.151+1G>T
ENST00000353468.4:c.151+1G>T	ENSP00000434453.1:n.151+1G>T
ENST00000378892.5:c.-242G>T	ENSP00000368170.1:n.-242G>T
ENST00000461426.1:n.251G>T
ENST00000477726.1:c.151+1G>T	ENSP00000420022.1:n.151+1G>T
ENST00000497006.1:n.137+1G>T
NM_001282205.1:c.151+1G>T	NP_001269134.1:n.151+1G>T
NM_001282206.1:c.-103+1G>T	NP_001269135.1:n.-103+1G>T
NM_001282207.1:c.91+61G>T	NP_001269136.1:n.91+61G>T
NM_001282208.1:c.151+1G>T	NP_001269137.1:n.151+1G>T
NM_001282209.1:c.151+1G>T	NP_001269138.1:n.151+1G>T
NM_005866.3:c.151+1G>T	NP_005857.1:n.151+1G>T
NM_147157.2:c.151+1G>T	NP_671513.1:n.151+1G>T
NR_104108.1:n.280+1G>T
XM_011517674.1:c.151+1G>T	XP_011515976.1:n.151+1G>T
NM_005866.4:c.151+1G>T MANE Select	NP_005857.1:n.151+1G>T
NM_001282205.2:c.151+1G>T	NP_001269134.1:n.151+1G>T
NM_001282206.2:c.-103+1G>T	NP_001269135.1:n.-103+1G>T
NM_001282207.2:c.91+61G>T	NP_001269136.1:n.91+61G>T
NM_001282208.2:c.151+1G>T	NP_001269137.1:n.151+1G>T
NM_001282209.2:c.151+1G>T	NP_001269138.1:n.151+1G>T
NM_147157.3:c.151+1G>T	NP_671513.1:n.151+1G>T
NR_104108.2:n.241+1G>T