Canonical Allele Identifier: CA2739561848

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524486G>C , CM000679.2:g.75524486G>C	GRCh38
NC_000017.10:g.73520567G>C , CM000679.1:g.73520567G>C	GRCh37
NC_000017.9:g.71032162G>C	NCBI36
NG_013041.1:g.12959G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*74G>C MANE Select	ENSP00000327487.6:n.*74G>C
ENST00000434205.8:c.*74G>C	ENSP00000406559.4:n.*74G>C
ENST00000545228.3:c.*154G>C	ENSP00000438169.3:n.*154G>C
ENST00000577197.2:n.853G>C
ENST00000579449.2:n.2395G>C
ENST00000580013.6:n.2799G>C
ENST00000679370.1:n.3177G>C
ENST00000679429.1:c.*1113G>C	ENSP00000505403.1:n.*1113G>C
ENST00000679443.1:n.1724G>C
ENST00000679782.1:c.*354G>C	ENSP00000505995.1:n.*354G>C
ENST00000679919.1:n.1926G>C
ENST00000679928.1:c.*2207G>C	ENSP00000506071.1:n.*2207G>C
ENST00000680999.1:c.*74G>C	ENSP00000504984.1:n.*74G>C
ENST00000681282.1:c.*1842G>C	ENSP00000506339.1:n.*1842G>C
ENST00000333213.10:c.*74G>C	ENSP00000327487.6:n.*74G>C
ENST00000545228.2:c.932G>C
ENST00000577197.1:n.403G>C
NM_207346.2:c.*74G>C	NP_997229.2:n.*74G>C
XM_005257229.2:c.*154G>C	XP_005257286.1:n.*154G>C
XM_006721821.2:c.*154G>C	XP_006721884.1:n.*154G>C
XM_011524616.1:c.*154G>C	XP_011522918.1:n.*154G>C
XM_011524618.1:c.*74G>C	XP_011522920.1:n.*74G>C
XR_243646.2:n.1887G>C
XM_005257229.4:c.*154G>C	XP_005257286.1:n.*154G>C
XR_243646.4:n.1893G>C
NM_207346.3:c.*74G>C MANE Select	NP_997229.2:n.*74G>C