Canonical Allele Identifier: CA69517537

Gene: TAMM41

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.11839221C>A , CM000665.2:g.11839221C>A	GRCh38
NC_000003.11:g.11880695C>A , CM000665.1:g.11880695C>A	GRCh37
NC_000003.10:g.11855695C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001284401.2:c.411+1G>T MANE Select	NP_001271330.1:n.411+1G>T
ENST00000455809.6:c.411+1G>T MANE Select	ENSP00000398596.1:n.411+1G>T
NM_001284401.1:c.411+1G>T	NP_001271330.1:n.411+1G>T
NM_001321294.1:c.288+1G>T	NP_001308223.1:n.288+1G>T
NM_001321294.2:c.288+1G>T	NP_001308223.1:n.288+1G>T
NM_001321295.1:c.-237+1G>T	NP_001308224.1:n.-237+1G>T
NM_001321295.2:c.-237+1G>T	NP_001308224.1:n.-237+1G>T
NM_001366031.1:c.411+1G>T	NP_001352960.1:n.411+1G>T
NM_001366031.2:c.411+1G>T	NP_001352960.1:n.411+1G>T
NM_001394474.1:c.411+1G>T	NP_001381403.1:n.411+1G>T
NM_138807.3:c.411+1G>T	NP_620162.1:n.411+1G>T
NM_138807.4:c.411+1G>T	NP_620162.1:n.411+1G>T
NR_104314.1:n.694+1G>T
NR_104314.2:n.660+1G>T
NR_135609.1:n.900+1G>T
NR_135609.2:n.866+1G>T
NR_135610.1:n.900+1G>T
NR_135610.2:n.866+1G>T
NR_135611.1:n.694+1G>T
NR_135611.2:n.660+1G>T
NR_158710.1:n.660+1G>T
NR_158711.1:n.660+1G>T
NR_158712.1:n.660+1G>T
NR_158713.1:n.660+1G>T
NR_158713.2:n.660+1G>T
NR_158714.1:n.660+1G>T
NR_158715.1:n.866+1G>T
NR_158715.2:n.866+1G>T
ENST00000273037.9:c.411+1G>T	ENSP00000273037.5:n.411+1G>T
ENST00000411947.1:c.411+1G>T	ENSP00000392289.1:n.411+1G>T
ENST00000417723.1:c.*293+1G>T	ENSP00000390910.1:n.*293+1G>T
ENST00000444133.6:c.411+1G>T	ENSP00000388598.2:n.411+1G>T
ENST00000455809.5:c.411+1G>T	ENSP00000398596.1:n.411+1G>T
ENST00000457498.5:c.411+1G>T	ENSP00000406054.1:n.411+1G>T
XM_005264873.2:c.411+1G>T	XP_005264930.1:n.411+1G>T
XM_005264873.4:c.411+1G>T	XP_005264930.1:n.411+1G>T
XM_005264875.2:c.411+1G>T	XP_005264932.1:n.411+1G>T
XM_005264875.4:c.411+1G>T	XP_005264932.1:n.411+1G>T
XM_011533358.1:c.288+1G>T	XP_011531660.1:n.288+1G>T
XM_011533359.1:c.411+1G>T	XP_011531661.1:n.411+1G>T
XM_011533360.1:c.-237+1G>T	XP_011531662.1:n.-237+1G>T
XM_017005725.2:c.411+1G>T	XP_016861214.1:n.411+1G>T
XM_017005726.2:c.411+1G>T	XP_016861215.1:n.411+1G>T
XM_017005727.1:c.-1142+1G>T	XP_016861216.1:n.-1142+1G>T
XR_001740020.2:n.656+1G>T
XR_001740021.2:n.656+1G>T
XR_427250.1:n.694+1G>T
XR_940378.1:n.694+1G>T
XR_940379.1:n.694+1G>T