Canonical Allele Identifier: CA2838305491

Gene: TNRC6C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78079361C>A , CM000679.2:g.78079361C>A	GRCh38
NC_000017.10:g.76075442C>A , CM000679.1:g.76075442C>A	GRCh37
NC_000017.9:g.73587037C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588061.6:c.3361-34C>A	ENSP00000468647.2:n.3361-34C>A
ENST00000696270.1:c.3832-34C>A MANE Select	ENSP00000512514.1:n.3832-34C>A
ENST00000696541.1:c.3832-34C>A	ENSP00000512702.1:n.3832-34C>A
ENST00000636222.1:c.3856-34C>A	ENSP00000489933.1:n.3856-34C>A
ENST00000301624.8:c.3211-34C>A	ENSP00000301624.4:n.3211-34C>A
ENST00000335749.4:c.3202-34C>A	ENSP00000336783.4:n.3202-34C>A
ENST00000588061.5:c.3211-34C>A	ENSP00000468647.1:n.3211-34C>A
ENST00000588847.5:c.3202-34C>A	ENSP00000467154.1:n.3202-34C>A
NM_001142640.1:c.3202-34C>A	NP_001136112.1:n.3202-34C>A
NM_018996.3:c.3211-34C>A	NP_061869.2:n.3211-34C>A
XM_005257547.3:c.3832-34C>A	XP_005257604.2:n.3832-34C>A
XM_005257548.3:c.3841-34C>A	XP_005257605.2:n.3841-34C>A
XM_006721996.2:c.3841-34C>A	XP_006722059.2:n.3841-34C>A
XM_006721997.2:c.3691-34C>A	XP_006722060.2:n.3691-34C>A
XM_006721999.2:c.3691-3686C>A	XP_006722062.2:n.3691-3686C>A
XM_006722000.2:c.3832-34C>A	XP_006722063.2:n.3832-34C>A
XM_011525088.1:c.3211-34C>A	XP_011523390.1:n.3211-34C>A
XM_006721996.4:c.3937-34C>A	XP_006722059.3:n.3937-34C>A
XM_006721997.4:c.3787-34C>A	XP_006722060.3:n.3787-34C>A
XM_006722000.4:c.3928-34C>A	XP_006722063.3:n.3928-34C>A
XM_011525088.2:c.3211-34C>A	XP_011523390.1:n.3211-34C>A
XM_017024906.1:c.3928-34C>A	XP_016880395.1:n.3928-34C>A
XM_017024907.1:c.3937-34C>A	XP_016880396.1:n.3937-34C>A
XM_024450848.1:c.3841-34C>A	XP_024306616.1:n.3841-34C>A
NM_001142640.2:c.3832-34C>A MANE Select	NP_001136112.2:n.3832-34C>A
NM_001395508.1:c.3202-34C>A	NP_001382437.1:n.3202-34C>A
NM_001395509.1:c.3856-34C>A	NP_001382438.1:n.3856-34C>A
NM_001395510.1:c.3832-34C>A	NP_001382439.1:n.3832-34C>A
NM_001395511.1:c.3226-34C>A	NP_001382440.1:n.3226-34C>A
NM_001395512.1:c.3202-34C>A	NP_001382441.1:n.3202-34C>A