Canonical Allele Identifier: CA2695206837
Community Standard Title: NM_006828.4(ASCC3):c.3522dup (p.Cys1175MetfsTer?)
Gene: ASCC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.100646727dup , CM000668.2:g.100646727dup GRCh38
NC_000006.11:g.101094603dup , CM000668.1:g.101094603dup GRCh37
NC_000006.10:g.101201324dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006828.4:c.3522dup MANE Select NP_006819.2:p.Cys1175MetfsTer?
ENST00000369162.7:c.3522dup MANE Select ENSP00000358159.2:p.Cys1175MetfsTer?
NM_006828.3:c.3522dup NP_006819.2:p.Cys1175MetfsTer?
ENST00000369162.6:c.3522dup ENSP00000358159.2:p.Cys1175MetfsTer?
XM_011535394.1:c.3537dup XP_011533696.1:p.Cys1180MetfsTer?
XM_011535394.3:c.3537dup XP_011533696.1:p.Cys1180MetfsTer?
XM_011535395.1:c.3228dup XP_011533697.1:p.Cys1077MetfsTer?
XM_011535395.3:c.3228dup XP_011533697.1:p.Cys1077MetfsTer?
XM_011535396.1:c.3228dup XP_011533698.1:p.Cys1077MetfsTer?
XM_011535396.3:c.3228dup XP_011533698.1:p.Cys1077MetfsTer?
XM_017010205.2:c.3228dup XP_016865694.1:p.Cys1077MetfsTer?
XM_017010206.2:c.2103dup XP_016865695.1:p.Cys702MetfsTer?
XM_024446316.1:c.2724dup XP_024302084.1:p.Cys909MetfsTer?