Canonical Allele Identifier: CA15194697
Gene: DIS3L2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232123872A>C , CM000664.2:g.232123872A>C GRCh38
NC_000002.11:g.232988582A>C , CM000664.1:g.232988582A>C GRCh37
NC_000002.10:g.232696826A>C NCBI36
NG_032572.1:g.167290A>C , LRG_534:g.167290A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325385.12:c.602-6747A>C MANE Select ENSP00000315569.7:n.602-6747A>C
ENST00000273009.10:c.602-6747A>C ENSP00000273009.6:n.602-6747A>C
ENST00000325385.11:c.602-6747A>C ENSP00000315569.7:n.602-6747A>C
ENST00000390005.9:c.602-6747A>C ENSP00000374655.5:n.602-6747A>C
ENST00000409307.5:c.602-6747A>C ENSP00000386799.1:n.602-6747A>C
ENST00000409401.7:c.602-6747A>C ENSP00000386594.3:n.602-6747A>C
ENST00000433430.5:c.661-6747A>C ENSP00000391175.1:n.661-6747A>C
ENST00000445090.5:c.602-6747A>C ENSP00000388999.1:n.602-6747A>C
ENST00000470087.1:n.592-6747A>C
NM_001257281.1:c.602-6747A>C NP_001244210.1:n.602-6747A>C
NM_001257282.1:c.602-6747A>C NP_001244211.1:n.602-6747A>C
NM_152383.4:c.602-6747A>C , LRG_534t1:c.602-6747A>C NP_689596.4:n.602-6747A>C
NR_046476.1:n.878-6747A>C
NR_046477.1:n.878-6747A>C
NM_001257281.2:c.602-6747A>C NP_001244210.1:n.602-6747A>C
NM_152383.5:c.602-6747A>C MANE Select NP_689596.4:n.602-6747A>C
NR_046476.2:n.748-6747A>C
NR_046477.2:n.748-6747A>C
NM_001257282.2:c.602-6747A>C NP_001244211.1:n.602-6747A>C
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