Canonical Allele Identifier: CA2639836771

Gene: TSEN54

Linked Data

• gnomAD v4: 17-75524689-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524689C>G , CM000679.2:g.75524689C>G	GRCh38
NC_000017.10:g.73520770C>G , CM000679.1:g.73520770C>G	GRCh37
NC_000017.9:g.71032365C>G	NCBI36
NG_013041.1:g.13162C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*277C>G MANE Select	ENSP00000327487.6:n.*277C>G
ENST00000434205.8:c.*277C>G	ENSP00000406559.4:n.*277C>G
ENST00000545228.3:c.*357C>G	ENSP00000438169.3:n.*357C>G
ENST00000577197.2:n.1056C>G
ENST00000579449.2:n.2598C>G
ENST00000580013.6:n.3002C>G
ENST00000679370.1:n.3380C>G
ENST00000679429.1:c.*1316C>G	ENSP00000505403.1:n.*1316C>G
ENST00000679443.1:n.1927C>G
ENST00000679782.1:c.*557C>G	ENSP00000505995.1:n.*557C>G
ENST00000679919.1:n.2129C>G
ENST00000679928.1:c.*2410C>G	ENSP00000506071.1:n.*2410C>G
ENST00000680999.1:c.*277C>G	ENSP00000504984.1:n.*277C>G
ENST00000681282.1:c.*2045C>G	ENSP00000506339.1:n.*2045C>G
ENST00000333213.10:c.*277C>G	ENSP00000327487.6:n.*277C>G
ENST00000545228.2:c.1135C>G
ENST00000577197.1:n.606C>G
NM_207346.2:c.*277C>G	NP_997229.2:n.*277C>G
XM_005257229.2:c.*357C>G	XP_005257286.1:n.*357C>G
XM_006721821.2:c.*357C>G	XP_006721884.1:n.*357C>G
XM_011524616.1:c.*357C>G	XP_011522918.1:n.*357C>G
XM_011524618.1:c.*277C>G	XP_011522920.1:n.*277C>G
XR_243646.2:n.2090C>G
XM_005257229.4:c.*357C>G	XP_005257286.1:n.*357C>G
XR_243646.4:n.2096C>G
NM_207346.3:c.*277C>G MANE Select	NP_997229.2:n.*277C>G