Canonical Allele Identifier: CA365114705
Community Standard Title: NM_006828.4(ASCC3):c.4690T>C (p.Ser1564Pro)
Gene: ASCC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.100625287A>G , CM000668.2:g.100625287A>G GRCh38
NC_000006.11:g.101073163A>G , CM000668.1:g.101073163A>G GRCh37
NC_000006.10:g.101179884A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006828.4:c.4690T>C MANE Select NP_006819.2:p.Ser1564Pro
ENST00000369162.7:c.4690T>C MANE Select ENSP00000358159.2:p.Ser1564Pro
NM_006828.3:c.4690T>C NP_006819.2:p.Ser1564Pro
ENST00000369162.6:c.4690T>C ENSP00000358159.2:p.Ser1564Pro
XM_011535394.1:c.4705T>C XP_011533696.1:p.Ser1569Pro
XM_011535394.3:c.4705T>C XP_011533696.1:p.Ser1569Pro
XM_011535395.1:c.4396T>C XP_011533697.1:p.Ser1466Pro
XM_011535395.3:c.4396T>C XP_011533697.1:p.Ser1466Pro
XM_011535396.1:c.4396T>C XP_011533698.1:p.Ser1466Pro
XM_011535396.3:c.4396T>C XP_011533698.1:p.Ser1466Pro
XM_017010205.2:c.4396T>C XP_016865694.1:p.Ser1466Pro
XM_017010206.2:c.3271T>C XP_016865695.1:p.Ser1091Pro
XM_024446316.1:c.3892T>C XP_024302084.1:p.Ser1298Pro