Canonical Allele Identifier: CA393640894
Community Standard Title: NM_020843.4(SCAPER):c.829C>T (p.Arg277Ter)
Gene: SCAPER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.76775061G>A , CM000677.2:g.76775061G>A GRCh38
NC_000015.9:g.77067402G>A , CM000677.1:g.77067402G>A GRCh37
NC_000015.8:g.74854457G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_020843.4:c.829C>T MANE Select NP_065894.2:p.Arg277Ter
ENST00000563290.6:c.829C>T MANE Select ENSP00000454973.1:p.Arg277Ter
NM_001145923.1:c.91C>T NP_001139395.1:p.Arg31Ter
NM_001145923.2:c.91C>T NP_001139395.1:p.Arg31Ter
NM_001353009.1:c.829C>T NP_001339938.1:p.Arg277Ter
NM_001353009.2:c.829C>T NP_001339938.1:p.Arg277Ter
NM_001353010.1:c.427C>T NP_001339939.1:p.Arg143Ter
NM_001353010.2:c.427C>T NP_001339939.1:p.Arg143Ter
NM_001353011.1:c.427C>T NP_001339940.1:p.Arg143Ter
NM_001353011.2:c.427C>T NP_001339940.1:p.Arg143Ter
NM_001353012.1:c.427C>T NP_001339941.1:p.Arg143Ter
NM_001353012.2:c.427C>T NP_001339941.1:p.Arg143Ter
NM_020843.2:c.829C>T NP_065894.2:p.Arg277Ter
NM_020843.3:c.829C>T NP_065894.2:p.Arg277Ter
NR_148227.1:n.1086C>T
NR_148227.2:n.969C>T
ENST00000303521.10:n.875C>T
ENST00000324767.11:c.829C>T ENSP00000326924.7:p.Arg277Ter
ENST00000538941.6:c.91C>T ENSP00000442190.2:p.Arg31Ter
ENST00000562890.1:n.542C>T
ENST00000563290.5:c.829C>T ENSP00000454973.1:p.Arg277Ter
ENST00000564022.1:c.4C>T ENSP00000456987.1:p.Arg2Ter
ENST00000564590.5:c.829C>T ENSP00000456508.1:p.Arg277Ter
ENST00000565507.5:c.*668C>T ENSP00000455623.1:n.*668C>T
ENST00000565970.5:c.829C>T ENSP00000455378.1:p.Arg277Ter
ENST00000567618.5:n.287C>T
ENST00000568549.5:c.277C>T ENSP00000457434.1:n.277C>T
XM_005254417.2:c.829C>T XP_005254474.1:p.Arg277Ter
XM_005254419.2:c.829C>T XP_005254476.1:p.Arg277Ter
XM_011521648.1:c.985C>T XP_011519950.1:p.Arg329Ter
XM_011521649.1:c.985C>T XP_011519951.1:p.Arg329Ter
XM_011521650.1:c.829C>T XP_011519952.1:p.Arg277Ter
XM_011521651.1:c.985C>T XP_011519953.1:p.Arg329Ter
XM_011521652.1:c.781C>T XP_011519954.1:p.Arg261Ter
XM_011521653.1:c.427C>T XP_011519955.1:p.Arg143Ter
XM_011521653.3:c.427C>T XP_011519955.1:p.Arg143Ter
XM_011521654.1:c.91C>T XP_011519956.1:p.Arg31Ter
XM_011521655.1:c.985C>T XP_011519957.1:p.Arg329Ter
XM_017022268.1:c.829C>T XP_016877757.1:p.Arg277Ter
XM_017022269.1:c.829C>T XP_016877758.1:p.Arg277Ter
XM_017022270.1:c.829C>T XP_016877759.1:p.Arg277Ter
XM_017022272.1:c.829C>T XP_016877761.1:p.Arg277Ter
XM_017022273.1:c.427C>T XP_016877762.1:p.Arg143Ter
XM_017022275.2:c.-15C>T XP_016877764.1:n.-15C>T
XM_017022276.1:c.-15C>T XP_016877765.1:n.-15C>T
XM_017022277.2:c.-15C>T XP_016877766.1:n.-15C>T
XM_017022278.2:c.-15C>T XP_016877767.1:n.-15C>T
XM_017022283.1:c.829C>T XP_016877772.1:p.Arg277Ter
XM_024449937.1:c.427C>T XP_024305705.1:p.Arg143Ter
XM_024449938.1:c.91C>T XP_024305706.1:p.Arg31Ter
XM_024449939.1:c.91C>T XP_024305707.1:p.Arg31Ter
XM_024449940.1:c.427C>T XP_024305708.1:p.Arg143Ter
XM_024449941.1:c.427C>T XP_024305709.1:p.Arg143Ter
XM_024449942.1:c.427C>T XP_024305710.1:p.Arg143Ter
XM_024449943.1:c.427C>T XP_024305711.1:p.Arg143Ter
XM_024449944.1:c.427C>T XP_024305712.1:p.Arg143Ter
XR_002957646.1:n.698C>T
XR_002957647.1:n.698C>T