Canonical Allele Identifier: CA627406679

Gene: TSEN54

Linked Data

• dbSNP Id: rs1317378521
• gnomAD v2: 17-73520682-A-G
• gnomAD v4: 17-75524601-A-G
• MyVariant Identifiers: chr17:g.73520682A>G (hg19) ; chr17:g.75524601A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524601A>G , CM000679.2:g.75524601A>G	GRCh38
NC_000017.10:g.73520682A>G , CM000679.1:g.73520682A>G	GRCh37
NC_000017.9:g.71032277A>G	NCBI36
NG_013041.1:g.13074A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*189A>G MANE Select	ENSP00000327487.6:n.*189A>G
ENST00000434205.8:c.*189A>G	ENSP00000406559.4:n.*189A>G
ENST00000545228.3:c.*269A>G	ENSP00000438169.3:n.*269A>G
ENST00000577197.2:n.968A>G
ENST00000579449.2:n.2510A>G
ENST00000580013.6:n.2914A>G
ENST00000679370.1:n.3292A>G
ENST00000679429.1:c.*1228A>G	ENSP00000505403.1:n.*1228A>G
ENST00000679443.1:n.1839A>G
ENST00000679782.1:c.*469A>G	ENSP00000505995.1:n.*469A>G
ENST00000679919.1:n.2041A>G
ENST00000679928.1:c.*2322A>G	ENSP00000506071.1:n.*2322A>G
ENST00000680999.1:c.*189A>G	ENSP00000504984.1:n.*189A>G
ENST00000681282.1:c.*1957A>G	ENSP00000506339.1:n.*1957A>G
ENST00000333213.10:c.*189A>G	ENSP00000327487.6:n.*189A>G
ENST00000545228.2:c.1047A>G
ENST00000577197.1:n.518A>G
NM_207346.2:c.*189A>G	NP_997229.2:n.*189A>G
XM_005257229.2:c.*269A>G	XP_005257286.1:n.*269A>G
XM_006721821.2:c.*269A>G	XP_006721884.1:n.*269A>G
XM_011524616.1:c.*269A>G	XP_011522918.1:n.*269A>G
XM_011524618.1:c.*189A>G	XP_011522920.1:n.*189A>G
XR_243646.2:n.2002A>G
XM_005257229.4:c.*269A>G	XP_005257286.1:n.*269A>G
XR_243646.4:n.2008A>G
NM_207346.3:c.*189A>G MANE Select	NP_997229.2:n.*189A>G