Canonical Allele Identifier: CA5170928

Gene: TMEM38B

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.105748063T>G , CM000671.2:g.105748063T>G	GRCh38
NC_000009.11:g.108510344T>G , CM000671.1:g.108510344T>G	GRCh37
NC_000009.10:g.107550165T>G	NCBI36
NG_032971.1:g.58539T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_018112.3:c.543-10T>G MANE Select	NP_060582.1:n.543-10T>G
ENST00000374692.8:c.543-10T>G MANE Select	ENSP00000363824.3:n.543-10T>G
NM_018112.2:c.543-10T>G	NP_060582.1:n.543-10T>G
ENST00000374688.5:c.381-10T>G	ENSP00000363820.1:n.381-10T>G
ENST00000374692.7:c.543-10T>G	ENSP00000363824.3:n.543-10T>G
ENST00000435034.5:c.353-10T>G
ENST00000451560.1:c.124-10T>G
XM_005252075.2:c.381-10T>G	XP_005252132.1:n.381-10T>G
XM_005252076.1:c.543-10T>G	XP_005252133.1:n.543-10T>G
XM_005252076.3:c.543-10T>G	XP_005252133.1:n.543-10T>G
XM_005252077.2:c.543-10T>G	XP_005252134.1:n.543-10T>G
XM_005252077.3:c.543-10T>G	XP_005252134.1:n.543-10T>G
XM_005252078.2:c.542+25442T>G	XP_005252135.1:n.542+25442T>G
XM_011518829.1:c.571-10T>G	XP_011517131.1:n.571-10T>G
XM_011518830.1:c.571-10T>G	XP_011517132.1:n.571-10T>G
XM_011518831.1:c.571-10T>G	XP_011517133.1:n.571-10T>G
XM_011518831.2:c.571-10T>G	XP_011517133.1:n.571-10T>G
XM_011518832.1:c.270-10T>G	XP_011517134.1:n.270-10T>G
XM_011518832.3:c.270-10T>G	XP_011517134.1:n.270-10T>G
XM_011518833.1:c.195-10T>G	XP_011517135.1:n.195-10T>G
XM_011518833.3:c.195-10T>G	XP_011517135.1:n.195-10T>G
XR_001746343.1:n.688-10T>G