Canonical Allele Identifier: CA502045850

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73517804C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521723C>A , CM000679.2:g.75521723C>A	GRCh38
NC_000017.10:g.73517804C>A , CM000679.1:g.73517804C>A	GRCh37
NC_000017.9:g.71029399C>A	NCBI36
NG_013041.1:g.10196C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000333213.11:c.642C>A MANE Select	ENSP00000327487.6:p.Ala214=
ENST00000434205.8:c.339C>A	ENSP00000406559.4:p.Ala113=
ENST00000545228.3:c.642C>A	ENSP00000438169.3:p.Ala214=
ENST00000579449.2:n.441C>A
ENST00000580013.6:n.845C>A
ENST00000583818.2:c.696C>A	ENSP00000461928.2:n.696C>A
ENST00000679370.1:n.1223C>A
ENST00000679429.1:c.*100C>A	ENSP00000505403.1:n.*100C>A
ENST00000679443.1:n.711C>A
ENST00000679782.1:c.642C>A	ENSP00000505995.1:p.Ala214=
ENST00000679919.1:n.711C>A
ENST00000679928.1:c.*253C>A	ENSP00000506071.1:n.*253C>A
ENST00000680528.1:n.667C>A
ENST00000680999.1:c.642C>A	ENSP00000504984.1:p.Ala214=
ENST00000681282.1:c.671C>A	ENSP00000506339.1:p.Pro224Gln
ENST00000333213.10:c.642C>A	ENSP00000327487.6:p.Ala214=
ENST00000578415.1:c.602C>A
ENST00000583173.5:c.458+213C>A	ENSP00000463619.1:n.458+213C>A
ENST00000583818.1:c.591C>A	ENSP00000461928.1:n.591C>A
NM_207346.2:c.642C>A	NP_997229.2:p.Ala214=
XM_005257229.2:c.642C>A	XP_005257286.1:p.Ala214=
XM_006721821.2:c.339C>A	XP_006721884.1:p.Ala113=
XM_011524616.1:c.642C>A	XP_011522918.1:p.Ala214=
XM_011524617.1:c.642C>A	XP_011522919.1:p.Ala214=
XM_011524618.1:c.642C>A	XP_011522920.1:p.Ala214=
XR_243646.2:n.672C>A
XM_005257229.4:c.642C>A	XP_005257286.1:p.Ala214=
XR_243646.4:n.678C>A
NM_207346.3:c.642C>A MANE Select	NP_997229.2:p.Ala214=