Canonical Allele Identifier: CA352188370

Gene: TTC21A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39114743G>A , CM000665.2:g.39114743G>A	GRCh38
NC_000003.11:g.39156234G>A , CM000665.1:g.39156234G>A	GRCh37
NC_000003.10:g.39131238G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001366900.1:c.716+1G>A MANE Select	NP_001353829.1:n.716+1G>A
ENST00000683103.1:c.716+1G>A MANE Select	ENSP00000507739.1:n.716+1G>A
NM_001105513.2:c.593+1G>A	NP_001098983.2:n.593+1G>A
NM_001105513.3:c.593+1G>A	NP_001098983.2:n.593+1G>A
NM_001366899.1:c.716+1G>A	NP_001353828.1:n.716+1G>A
NM_145755.2:c.716+1G>A	NP_665698.2:n.716+1G>A
NM_145755.3:c.716+1G>A	NP_665698.2:n.716+1G>A
NR_159494.1:n.874+1G>A
NR_159495.1:n.874+1G>A
NR_159496.1:n.874+1G>A
ENST00000430597.6:c.716+1G>A	ENSP00000405396.2:n.716+1G>A
ENST00000431162.6:c.716+1G>A	ENSP00000398211.2:n.716+1G>A
ENST00000431559.5:c.315+1G>A	ENSP00000395118.1:n.315+1G>A
ENST00000440121.1:c.593+1G>A	ENSP00000410882.1:n.593+1G>A
ENST00000459702.1:n.577+1G>A
ENST00000479954.5:n.837+1G>A
ENST00000493337.5:n.423+1G>A
XM_005264921.3:c.716+1G>A	XP_005264978.1:n.716+1G>A
XM_005264921.5:c.716+1G>A	XP_005264978.1:n.716+1G>A
XM_005264922.3:c.716+1G>A	XP_005264979.1:n.716+1G>A
XM_005264922.5:c.716+1G>A	XP_005264979.1:n.716+1G>A
XM_005264923.2:c.716+1G>A	XP_005264980.1:n.716+1G>A
XM_005264924.3:c.716+1G>A	XP_005264981.1:n.716+1G>A
XM_005264924.5:c.716+1G>A	XP_005264981.1:n.716+1G>A
XM_005264925.3:c.593+1G>A	XP_005264982.1:n.593+1G>A
XM_005264925.5:c.593+1G>A	XP_005264982.1:n.593+1G>A
XM_005264926.3:c.716+1G>A	XP_005264983.1:n.716+1G>A
XM_005264926.5:c.716+1G>A	XP_005264983.1:n.716+1G>A
XM_005264927.3:c.155+1G>A	XP_005264984.1:n.155+1G>A
XM_005264927.4:c.155+1G>A	XP_005264984.1:n.155+1G>A
XM_006713011.2:c.716+1G>A	XP_006713074.1:n.716+1G>A
XM_006713011.4:c.716+1G>A	XP_006713074.1:n.716+1G>A
XM_006713012.2:c.716+1G>A	XP_006713075.1:n.716+1G>A
XM_011533447.1:c.716+1G>A	XP_011531749.1:n.716+1G>A
XM_011533447.3:c.716+1G>A	XP_011531749.1:n.716+1G>A
XM_011533449.1:c.716+1G>A	XP_011531751.1:n.716+1G>A
XM_011533449.2:c.716+1G>A	XP_011531751.1:n.716+1G>A
XM_017005843.2:c.716+1G>A	XP_016861332.1:n.716+1G>A
XM_024453382.1:c.716+1G>A	XP_024309150.1:n.716+1G>A
XR_001740049.2:n.831+1G>A
XR_001740050.2:n.831+1G>A
XR_245099.2:n.843+1G>A
XR_427256.2:n.843+1G>A
XR_427256.3:n.831+1G>A
XR_427257.2:n.843+1G>A
XR_427257.3:n.831+1G>A
XR_940387.1:n.843+1G>A