Canonical Allele Identifier: CA627406568

Gene: TSEN54

Linked Data

• dbSNP Id: rs1193461677
• gnomAD v2: 17-73520087-G-C
• gnomAD v3: 17-75524006-G-C
• gnomAD v4: 17-75524006-G-C
• MyVariant Identifiers: chr17:g.73520087G>C (hg19) ; chr17:g.75524006G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524006G>C , CM000679.2:g.75524006G>C	GRCh38
NC_000017.10:g.73520087G>C , CM000679.1:g.73520087G>C	GRCh37
NC_000017.9:g.71031682G>C	NCBI36
NG_013041.1:g.12479G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1430+227G>C MANE Select	ENSP00000327487.6:n.1430+227G>C
ENST00000434205.8:c.1127+227G>C	ENSP00000406559.4:n.1127+227G>C
ENST00000545228.3:c.1618+227G>C	ENSP00000438169.3:n.1618+227G>C
ENST00000577197.2:n.628+227G>C
ENST00000579449.2:n.2170+227G>C
ENST00000580013.6:n.2574+227G>C
ENST00000679370.1:n.2952+227G>C
ENST00000679429.1:c.*888+227G>C	ENSP00000505403.1:n.*888+227G>C
ENST00000679443.1:n.1499+227G>C
ENST00000679782.1:c.*129+227G>C	ENSP00000505995.1:n.*129+227G>C
ENST00000679919.1:n.1701+227G>C
ENST00000679928.1:c.*1982+227G>C	ENSP00000506071.1:n.*1982+227G>C
ENST00000680528.1:n.2396+227G>C
ENST00000680999.1:c.1643+227G>C	ENSP00000504984.1:n.1643+227G>C
ENST00000681282.1:c.*1617+227G>C	ENSP00000506339.1:n.*1617+227G>C
ENST00000333213.10:c.1430+227G>C	ENSP00000327487.6:n.1430+227G>C
ENST00000545228.2:c.707+227G>C
ENST00000577197.1:n.178+227G>C
ENST00000579449.1:n.627+227G>C
NM_207346.2:c.1430+227G>C	NP_997229.2:n.1430+227G>C
XM_005257229.2:c.1618+227G>C	XP_005257286.1:n.1618+227G>C
XM_006721821.2:c.1315+227G>C	XP_006721884.1:n.1315+227G>C
XM_011524616.1:c.1502-256G>C	XP_011522918.1:n.1502-256G>C
XM_011524617.1:c.*13-256G>C	XP_011522919.1:n.*13-256G>C
XM_011524618.1:c.1314-256G>C	XP_011522920.1:n.1314-256G>C
XR_243646.2:n.1662+227G>C
XM_005257229.4:c.1618+227G>C	XP_005257286.1:n.1618+227G>C
XR_001753015.1:n.87+305C>G
XR_001753016.1:n.88+305C>G
XR_243646.4:n.1668+227G>C
NM_207346.3:c.1430+227G>C MANE Select	NP_997229.2:n.1430+227G>C