Canonical Allele Identifier: CA212767
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 1370
ClinVar RCV Id: RCV000001435
dbSNP Id: rs386834187
gnomAD v4: 8-93791320-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93791320G>A , CM000670.2:g.93791320G>A GRCh38
NC_000008.10:g.94803548G>A , CM000670.1:g.94803548G>A GRCh37
NC_000008.9:g.94872724G>A NCBI36
NG_009190.1:g.41477G>A , LRG_688:g.41477G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000323130.8:c.1575+1G>A ENSP00000314488.4:n.1575+1G>A
ENST00000409623.8:c.1530+1G>A ENSP00000386966.4:n.1530+1G>A
ENST00000452276.6:c.1575+1G>A ENSP00000388671.2:n.1575+1G>A
ENST00000453906.6:c.693+1G>A ENSP00000403035.2:n.693+1G>A
ENST00000520680.2:c.1575+1G>A ENSP00000428785.2:n.1575+1G>A
ENST00000521517.6:c.1575+1G>A ENSP00000430740.2:n.1575+1G>A
ENST00000681998.1:c.1396+1G>A ENSP00000506773.1:n.1396+1G>A
ENST00000682036.1:c.693+1G>A ENSP00000508390.1:n.693+1G>A
ENST00000682577.1:c.1348+1G>A ENSP00000506963.1:n.1348+1G>A
ENST00000682624.1:c.*1149+1G>A ENSP00000508343.1:n.*1149+1G>A
ENST00000682700.1:c.1575+1G>A ENSP00000507627.1:n.1575+1G>A
ENST00000682744.1:n.1113+1G>A
ENST00000682804.1:n.1398+1G>A
ENST00000682837.1:c.1064+1G>A ENSP00000507920.1:n.1064+1G>A
ENST00000682935.1:n.3625+1G>A
ENST00000682984.1:c.1236+1G>A ENSP00000507209.1:n.1236+1G>A
ENST00000683078.1:c.1330+1G>A ENSP00000506796.1:n.1330+1G>A
ENST00000683223.1:c.1307+1G>A ENSP00000507685.1:n.1307+1G>A
ENST00000683238.1:n.2799+1G>A
ENST00000683249.1:n.3172+1G>A
ENST00000683336.1:c.1396+1G>A ENSP00000507695.1:n.1396+1G>A
ENST00000683362.1:c.1236+1G>A ENSP00000506985.1:n.1236+1G>A
ENST00000683850.1:n.1498+1G>A
ENST00000683919.1:c.1505+1G>A ENSP00000507617.1:n.1505+1G>A
ENST00000683953.1:c.1486+1G>A ENSP00000508375.1:n.1486+1G>A
ENST00000684023.1:c.1552+1G>A ENSP00000507461.1:n.1552+1G>A
ENST00000684064.1:c.1266+1G>A ENSP00000508192.1:n.1266+1G>A
ENST00000684089.1:n.3125+1G>A
ENST00000684149.1:c.*754+1G>A ENSP00000507943.1:n.*754+1G>A
ENST00000684416.1:n.1534+1G>A
ENST00000684540.1:c.1505+1G>A ENSP00000507987.1:n.1505+1G>A
ENST00000453321.8:c.1575+1G>A MANE Select ENSP00000389998.3:n.1575+1G>A
ENST00000323130.7:c.1545+1G>A ENSP00000314488.3:n.1545+1G>A
ENST00000409623.7:c.1332+1G>A ENSP00000386966.3:n.1332+1G>A
ENST00000453321.7:c.1575+1G>A ENSP00000389998.3:n.1575+1G>A
ENST00000474944.5:n.713+1G>A
ENST00000520680.1:c.397+1G>A
ENST00000523230.5:n.110+1G>A
NM_001142301.1:c.1332+1G>A , LRG_688t2:c.1332+1G>A NP_001135773.1:n.1332+1G>A
NM_153704.5:c.1575+1G>A , LRG_688t1:c.1575+1G>A NP_714915.3:n.1575+1G>A
NR_024522.1:n.1646+1G>A
XM_006716686.2:c.1272+1G>A XP_006716749.1:n.1272+1G>A
XM_006716687.2:c.975+1G>A XP_006716750.1:n.975+1G>A
XM_011517363.1:c.693+1G>A XP_011515665.1:n.693+1G>A
XR_428387.1:n.1633+1G>A
XR_928360.1:n.1633+1G>A
XR_928361.1:n.1633+1G>A
XR_928362.1:n.1633+1G>A
XM_006716686.4:c.1272+1G>A XP_006716749.1:n.1272+1G>A
XM_011517363.3:c.693+1G>A XP_011515665.1:n.693+1G>A
XM_024447326.1:c.921+1G>A XP_024303094.1:n.921+1G>A
XR_001745619.2:n.1616+1G>A
XR_428387.2:n.1616+1G>A
XR_928360.3:n.1616+1G>A
XR_928362.3:n.1616+1G>A
NM_153704.6:c.1575+1G>A MANE Select NP_714915.3:n.1575+1G>A
NR_024522.2:n.1596+1G>A