Canonical Allele Identifier: CA502046184
Gene: TSEN54 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.73518105C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75522024C>T , CM000679.2:g.75522024C>T GRCh38
NC_000017.10:g.73518105C>T , CM000679.1:g.73518105C>T GRCh37
NC_000017.9:g.71029700C>T NCBI36
NG_013041.1:g.10497C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.943C>T MANE Select ENSP00000327487.6:p.Leu315=
ENST00000434205.8:c.640C>T ENSP00000406559.4:p.Leu214=
ENST00000545228.3:c.943C>T ENSP00000438169.3:p.Leu315=
ENST00000579449.2:n.742C>T
ENST00000580013.6:n.1146C>T
ENST00000679370.1:n.1524C>T
ENST00000679429.1:c.*401C>T ENSP00000505403.1:n.*401C>T
ENST00000679443.1:n.1012C>T
ENST00000679782.1:c.943C>T ENSP00000505995.1:p.Leu315=
ENST00000679919.1:n.1012C>T
ENST00000679928.1:c.*554C>T ENSP00000506071.1:n.*554C>T
ENST00000680528.1:n.968C>T
ENST00000680999.1:c.943C>T ENSP00000504984.1:p.Leu315=
ENST00000681282.1:c.*189C>T ENSP00000506339.1:n.*189C>T
ENST00000333213.10:c.943C>T ENSP00000327487.6:p.Leu315=
ENST00000545228.2:c.32C>T
ENST00000578415.1:c.903C>T
ENST00000583173.5:c.476C>T ENSP00000463619.1:p.Ser159Phe
NM_207346.2:c.943C>T NP_997229.2:p.Leu315=
XM_005257229.2:c.943C>T XP_005257286.1:p.Leu315=
XM_006721821.2:c.640C>T XP_006721884.1:p.Leu214=
XM_011524616.1:c.943C>T XP_011522918.1:p.Leu315=
XM_011524617.1:c.943C>T XP_011522919.1:p.Leu315=
XM_011524618.1:c.943C>T XP_011522920.1:p.Leu315=
XR_243646.2:n.973C>T
XM_005257229.4:c.943C>T XP_005257286.1:p.Leu315=
XR_243646.4:n.979C>T
NM_207346.3:c.943C>T MANE Select NP_997229.2:p.Leu315=