Canonical Allele Identifier: CA1586231750

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139273911C= , CM000667.2:g.139273911C= GRCh38
NC_000005.9:g.138609600C= , CM000667.1:g.138609600C= GRCh37
NC_000005.8:g.138637499C= NCBI36
NG_012846.1:g.4809C=

Transcript Alleles

HGVS Amino-acid change
ENST00000506147.5:c.-269C= ENSP00000423521.1:n.-269C=
ENST00000508744.1:n.466-257G= (SIL1)
ENST00000509400.5:n.293+6657G= (SIL1)
ENST00000509990.5:c.-537C= ENSP00000423533.1:n.-537C=
ENST00000512107.5:c.-486C= ENSP00000423695.1:n.-486C=
NM_001194954.1:c.-537C= (MATR3) NP_001181883.1:n.-537C=
NM_001282278.1:c.-544C= (MATR3) NP_001269207.1:n.-544C=
NM_199189.2:c.-619C= (MATR3) NP_954659.1:n.-619C=
NR_003141.3:n.160C= (SNHG4)
NR_036536.1:n.160C= (SNHG4)